Lediga jobb Astrazeneca AB i Göteborg

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.



What you will do

This is an opportunity for an engaged individual to join our Clinical Pharmacology and Quantitative Pharmacology (CPQP) team at AstraZeneca in Gothenburg (Sweden) and contribute as a Senior Scientist/Associate Director Clinical Pharmacology Scientist, supporting large and small molecule projects across all phases of clinical development within the therapy area of Cardiovascular Renal and Metabolism.

You will work closely with clinical pharmacometricians, physicians and other scientists, and apply your expertise and leadership skills to contribute to the strategy of the clinical program and the design and interpretation of clinical studies. You will influence key decisions in early and late phases of clinical development. Accountable for expert data integration, analysis, interpretation, and reporting of clinical pharmacology results at the study level in compliance with Good Clinical Practice (GCP) regulations. Jointly accountable with the clinical pharmacometrician for providing a scientific justification for the dose selection, for representing Clinical Pharmacology and Quantitative Pharmacology in cross-functional project teams, and for developing the clinical pharmacology strategy. Participation in and accountability for peer review of ongoing activities, reports and presentations. Contribute to regulatory documents and interactions (written and oral), present Clinical Pharmacology results within and outside of AstraZeneca and publish in peer reviewed journals. You will also contribute to internal initiatives to develop the clinical pharmacology field including its processes.



Essential requirements for this role

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PhD degree in clinical pharmacology, pharmacometrics or other relevant area
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Knowledge of pharmacokinetics, drug metabolism, and their clinical application
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Strategic knowledge and experience in the use of PK and PKPD modelling applied to life sciences
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Knowledge in pharmacology and drug targets
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Biological understanding of disease and drug action in the therapy area of Cardiovascular Renal and Metabolism
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Good oral and written communication skills



Desirable requirements

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At least 3 years industry experience or equivalent in pharmacokinetics and clinical pharmacology aspects of drug development (position level depends on overall years of proven experience)
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Early and late phase clinical development experience
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Track record in creating and delivering on clinical pharmacology strategies of both small and large molecules
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Recognized clinical pharmacology expert as demonstrated by scientific publishing in the field of clinical pharmacology
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Skills and experience in the use of PK and PKPD modeling tools such as Phoenix Winnonlin, NONMEM, R applied to life sciences



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.


So, what's next?

If you're ready to make a meaningful, lasting impact, apply today and help us push the boundaries of science to transform medicine.

Please submit your application, ideally including both a resume and a cover letter, by November 23, 2025. We review applications on a rolling basis, so we encourage you to apply as soon as possible. Visa mindre

At AstraZeneca, every employee plays a vital role in delivering life-changing medicines. Step into a Senior Administrator role at our Gothenburg site where your impact is felt every day. You'll keep leaders focused on delivering innovative, life?saving medicines by steering the complex demands of their business with clarity and confidence. Your work is the backbone of our ambitious mission, and success depends on the skills, initiative, and collaboration you bring to our dedicated team. If you thrive in fast-moving environments and love making things run smoothly, this is where your strengths will shine-right here at our vibrant site in Gothenburg.

About the Role

The Senior Administrator within Global Portfolio and Project Management (GPPM) will work closely with executive leaders across the world, supporting our BioPharma team and making a real impact every day. It's a dynamic role where your agility, initiative, and calm under pressure will shine-juggling evolving priorities, solving problems before they escalate, and building strong relationships across AstraZeneca. If you value discretion, enjoy fast-paced teamwork, and love bringing structure and positivity to complex environments, this is a place where you'll thrive and grow. You are championing a vibrant, fun culture where people feel supported, energized, and able to do their best work

Key Responsibilities

* Support coordination of the GPPM BioPharma leadership team, including setting agendas, preparing meetings, setting annual calendars etc.
* Provide all-round administrative support-scheduling, travel, expenses, purchase orders, meeting logistics, and document management-across multiple leaders and teams.
* Assist with new employee and leader onboarding/offboarding.
* Point of contact for functional engagement activities incl supporting global / local events.
* Maintain and circulate key information using collaboration platforms such as SharePoint, OneNote, and other systems.
* Organize and troubleshoot complex, multi-site meetings using platforms such as VMR, and Teams. Adopt new systems, technologies, and working practices as they emerge.
* Liaise with global AZ locations and admin counterparts to ensure efficient collaboration across GPPM and Enterprise partners e.g. R&D functions.

Essential Experience

* Extensive experience supporting senior leaders in a global organization including experience in VP level calendar management.
* Experience in implementing information management strategies and collaboration tools at functional level.
* Advanced proficiency across administrative systems such as Microsoft 365 apps and tools.
* Proven ability to manage confidential information and shifting priorities with minimal supervision.
* Collaborative, professional, and adaptable in fast-paced environments.
* Event and task management capabilities; comfortable learning new technology.

Desirable Experience

* Background in pharmaceuticals or drug development.
* Experience supporting large leadership or governance meetings.
* Expert with OneNote, Teams, Concur, or similar collaborative and travel systems.
* Administrative qualifications or knowledge of drug development processes.



Join us and be a key part of a collaborative, high-impact team making a real difference for patients worldwide!

Apply with your Cover letter and CV no later than November 2nd, 2025. Visa mindre

Are you motivated by using your data science skills to drive biological insights and are seeking a role where your expertise can make an extraordinary impact? This is an opportunity to join a dynamic and enthusiastic environment, whilst delivering critical support to drug discovery projects.



Join a place built on innovation and creativity. We harness digital, data science & AI to fast-forward our research. Making sure work born in a lab can make a real difference. Every day, impacting patients' lives across the world.



As a Director, Biostatistics and Informatics, you'll be part of the Data Sciences & Quantitative Biology department within Discovery Sciences - a global, diverse and delivery focused department where we collaborate to support drug projects aiming to impact patients' lives. In partnership with our experimentalist colleagues and other data scientists, we provide computational analysis and solutions to enable and enhance output from our technical platforms driving our drug discovery efforts. The role is based at our vibrant R&D site in Gothenburg, Sweden.



What you'll do

You will lead, mentor and develop the team and collaborate across functions to evolve our computational approaches and their drug discovery applications, to drive impact and deepen scientific excellence. We will rely on you to initiate and lead both internal and external collaborations and partnerships to ensure that we are at the cutting edge of technology and innovation.


We truly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues, mentors and leaders, will ensure you maximise your potential and contribution, building from your current skills, abilities and experience.


Essential for the role

Our team is a highly collaborative group of scientists, working in a constantly evolving technical and scientific landscape. Therefore, you'll have to be comfortable working at a fast pace, with a team-focused approach. You have excellent communication skills and a proactive and delivery-focused approach.


Regardless of your current level of leadership experience, you're passionate about supporting your staff and wider colleagues' development, as well as driving your own personal development and maximising your team's and individual contribution to drug discovery.


You also have:

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PhD, or equivalent, in bioinformatics, mathematics, computer science, statistics, engineering or the life sciences
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Expertise in omics, particularly NGS based technologies
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Expertise in biostatistics including Frequentist statistics, Bayesian statistics and Design of Experiments
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In-depth experience with drug discovery and AZ R&D disease area priorities and proven experience with impacting drug discovery projects across multiple disease areas.
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In-depth experience with delivering statistical solutions to early drug discovery
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In-depth experience of manipulating and analysing large high dimensionality unstructured datasets, drawing conclusions, defining recommended actions, and reporting results across stakeholders
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Excellent written and verbal communication, business analysis, and consultancy skills
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Experience in a complex global organization
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A track record of people leadership



Desirable for the role

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Comfortable working in high performance computing or cloud environment
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Proven track record of publishing relevant results and tools in peer-reviewed journals, conferences, and other scientific proceedings.
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Experience in novel methods development and application
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Experience in influencing and controlling budgets



The successful candidate can operate effectively in a multi-disciplinary research environment. You enjoy teamwork, have a collaborative nature and will be an encouraging colleague to all.



Work policy
When we put people in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. This role is located in Gothenburg, Sweden and is not available for remote work or with travel support.

What's next?
If this sound like the position and place for you - apply today!
We look forward to receiving your application, but no later than November 10, 2025. The interview process will be ongoing, do not hesitate to apply early.

More information
For more information about the position please contact the hiring manager Natalie van Zuydam, [email protected]

Additional information
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Life in Gothenburg: https://www.movetogothenburg.com/
About AstraZeneca R&D: https://www.astrazeneca.com/r-d.html Visa mindre

Are you a passionate Scientist with expertise in synthetic chemistry and have a great interest in the development of Oligonucleotide Therapeutics? Do you wish to join a growing team where you will have the opportunity to further exploit our drug discovery platforms? If yes, we have just the position for you at AstraZeneca, Discovery Sciences in Gothenburg, Sweden!

We are currently recruiting a motivated Senior Research Scientist with recognized solid support synthesis expertise within the oligonucleotide or peptide chemistry field to join our Oligonucleotide Chemistry team within the Oligonucleotide Discovery Department, part of the Discovery Sciences R&D organization at AstraZeneca in Gothenburg, Sweden.

This is an opportunity for you to apply your expert synthetic organic chemistry knowledge to expand the use of oligonucleotides, and molecular conjugates thereof, in the treatment of diseases across therapy areas within AstraZeneca. In doing so you demonstrate a passion for driving scientific questions, combined with strong working ethics and the ability to work well within teams aiming to drive drug discovery projects forward.

The Oligonucleotide Chemistry team is working in close collaboration with other Scientists in Discovery Sciences, Medicinal Chemistry, Pharmacology, DMPK, Safety and Pharmaceutical sciences with a focus on the goal to design and develop the oligonucleotide therapeutics of the future. We offer a highly rewarding scientific environment, with the expectation to publish new findings.

What you will do:
This role is a synthesis specialist role with a focus on developing oligonucleotide drugs and thereby supporting the AstraZeneca pipeline. You will also synthesize and purify high quality building blocks and compounds by applying cutting-edge technologies and methodologies to support project progression from pre-TSID to CDID according to agreed timelines, as well as applying purification and analytical sciences, troubleshoot challenges and make a significant contribution to the practical delivery of project compounds. You will work alongside other chemists in the team to support project priorities but should also be comfortable in supervising more junior colleagues. The role also includes development of new building blocks and linkers as well as setting up new techniques.

As a Senior Research Scientist you will propose experimental strategies and have the possibility to be creative in solving a wide range of synthetic challenges. You will plan, prioritize and perform your own work and actively collaborate with the project team by driving problem solving using literature and own knowledge. An important responsibility is to support oligonucleotide projects to ensure high scientific standards and quality of compounds to meet project objectives. You will build strong collaborative relationships within the team and in projects to ensure the smooth running of projects.


Essential requirements for the role:

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PhD in Organic Chemistry
*

Detailed knowledge of synthetic chemistry related to oligonucleotides, oligo building blocks and/or synthesis of advanced organic molecules
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Ability to design and execute experiments autonomously
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Evidence of experimental impact by either peer-reviewed publications or external presentations



The successful candidate will demonstrate a passion for driving scientific questions and is a scientifically critical individual capable of receiving and analysing input from multiple fields and deciding on focused course of action. You should also be able to work independently and have a positive, result-oriented, and problem-solving attitude. Excellent English is required, both spoken and written, and ability to operate effectively in a multi-disciplinary research environment. We also believe that you enjoy teamwork, have a collaborative nature and will be an encouraging colleague to all.



Desirable requirements for the role:

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Knowledge in the area of oligonucleotide therapeutics, design and data analysis
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Post-doc



Why AstraZeneca?
Our Gothenburg site is one of AstraZeneca's strategic science centres. We thrive in a multinational environment working cross-functionally across the globe with AstraZeneca colleagues as well as academic and industry partners. Our way of life is to develop a working environment that fosters collaboration, openness, and innovation. Therefore, we have built space for meetings, and socializing, where spontaneous meetings can give birth to new innovations.



What's next?

Does this sound like your next challenge and a good workplace for you? Welcome to apply today! We look forward to your application, no later than October 31, 2025. Visa mindre

Are you an expert in the skeletal muscle biology? Would you like to apply your research expertise to accelerating innovative science and turn ideas into life changing medicines? Join us to discover future treatments of Cardiovascular, Renal and Metabolic (CVRM) diseases!

We are seeking a passionate and accomplished Principal Scientist with expertise in skeletal muscle physiology, metabolism and drug discovery to join our vibrant research community Metabolism Bioscience Team within Research and Early Development CVRM. The position is primarily based at AstraZeneca's dynamic R&D site in Gothenburg, Sweden. For exceptional candidates, placement at our Cambridge, UK site may be considered.

CVRM is one of the three main therapeutic research areas within BioPharmaceuticals AstraZeneca which deliver candidate drugs into clinical development. The CVRM Bioscience department has a dynamic environment that fosters collaboration and innovation. We are a team of professionals who are passionate about advancing science to discover and develop novel therapeutics that will benefit patients suffering from obesity, diabetes and their co-morbidities.


Accountabilities
This scientific leadership role offers an exciting opportunity to set strategic direction and shape the future of obesity and weight management, with a focus on mechanisms underlying healthy body weight loss and maintenance. You will:

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Apply your expertise in skeletal muscle physiology and metabolic diseases to drive scientific and technical innovation, advancing new therapeutic interventions.
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Lead multidisciplinary project teams across Cambridge (UK), Gothenburg (Sweden), and Gaithersburg (US), as well as external collaborators, to deliver key experimental data and progress the drug project portfolio.
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Champion novel approaches to drug discovery in healthy weight loss and body weight maintenance, facilitating scientific debate and innovation through leadership and mentorship within the CVRM Research community.
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Contribute to the evolution of research strategy within the Metabolism Bioscience division as a member of its leadership team.
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Play a lead role in the selection and validation of research targets, taking projects from discovery through to early clinical development, and serve as bioscience lead on discovery projects.
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Raise the scientific profile of CVRM both internally and externally through high-impact publications, conference presentations, and collaborative initiatives.
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Report directly to the Senior Director of Metabolism Bioscience.

Essential Skills/Experience

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PhD and postdoctoral experience in life sciences or equivalent relevant industry experience.
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5+ years' drug discovery experience in academia, biotech, or pharmaceutical industry following postdoctoral research.
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Deep expertise in skeletal muscle biology and physiology, including in vitro and in vivo assay development.
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Extensive scientific knowledge of metabolic diseases and mechanisms of body weight regulation, alongside a strong track record of leading laboratory-based research.
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Experience in new model development, laboratory techniques, and enthusiasm for hands-on science.
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Demonstrated scientific leadership reflected by a robust publication record, external presentations, and collaborations.
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Proven ability to manage multifaceted projects and establish research collaborations, leveraging a broad professional network.
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Track record as a project leader or bioscience lead, conducting, planning, and guiding complex scientific projects within multidisciplinary teams.



Desirable Skills/Experience

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Significant experience with in vitro, in vivo, and ex vivo technologies to assess multiple target classes.
*

Ability to manage multiple concurrent projects or tasks.
*

Extensive network and collaboration experience within the obesity metabolism research field.



AstraZeneca is committed to making a difference by fusing data and technology with scientific innovations to achieve breakthroughs. We empower our teams to explore the biology of complex diseases, making bold decisions without fear of failure. Our inclusive environment fosters collaboration across academia, biotechs, and industry, leveraging diverse global knowledge for swift impact on disease. With opportunities for continuous learning and career development, AstraZeneca is where curious minds thrive as we push the boundaries of science to deliver life-changing medicines.

Ready to make an impact? Apply now to join our team! Welcome with your application no later than 19 October 2025. Visa mindre

Are you ready to make a significant impact in the world of pharmaceuticals? We have a great opportunity for a Packaging Technologist within our Pharmaceutical Technology and Development (PT&D) department.

This role is pivotal in supporting our entire PT&D product and packaging portfolio, transforming groundbreaking science into medicines that improve lives.

PT&D, within AstraZeneca Operations, spans the entire value chain, providing essential ingredients, formulations, and devices for new medicines, from early toxicology studies to clinical trials and scaling up drug production.

The role

As a Packaging Technologist, you will lead packaging development across our diverse product portfolio, with a focus on Oral Solid Dose packaging. Your expertise will be crucial in areas such as pharmaceutics, analytical sciences, validation science knowledge management, product robustness, analytics, process engineering, and technology enablement.

Collaborating closely with our packing partners in commercial operations, you will drive sustainability, design methodology, and standardization. You will also play a key role in delivering our packaging strategy in a dynamic, multi-skilled environment.



Key responsibilities include:

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Packaging support to our clinical and development product portfolio, applying specialist knowledge and expertise to achieve project targets in a timely fashion and to agreed quality standards
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Leading multi-functional packaging projects across AstraZeneca and partner organisations and being the point of contact to technically assess proposed pack changes and influence decision making.
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Ensuring that work is performed in accordance with appropriate safety (SHE), quality and compliance standards, e.g. GMP, and having the ability to understand and interpret packaging regulations.
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Generating and reviewing regulatory submission documents, project plans, protocols and technical reports ensuring that the project objectives are met
*

Use your technical expertise to support our packaging strategy in materials sourcing, asset transfers, capacity expansion, and manage the packaging product lifecycle with lean and six sigma methodologies.
*

Provide leadership in the implementation of digital tools into the packaging development process

Essential Skills/Experience:

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Bachelor's degree or equivalent experience in engineering, (Packaging or Mechanical Engineering preferred) or closely related field
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Able to demonstrate understanding of the principles and concepts in relation to pharmaceutical packaging
*

Is a recognised leader with direct experience and project management in an array of packaging aspects in one or more of the following: materials and polymer science, design methodology, sustainability, pharmaceutical packaging regulations and testing requirements, qualification and validation of new materials, product technical transfer and patient focussed packaging.
*

Has a working understanding and experience of one or more of the following: AutoCAD, SolidWorks, computer aided engineering (FEA, Computational / conversational fluid dynamics), product data management, rapid prototyping.
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Demonstrated ability to lead multi-functional teams across a global platform working with internal and external partners including contract manufacturers, vendors and academia while being able to hold a large degree of independence representing own department or area of expertise
*

Experience of working with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. Good Manufacturing Practice (GMP)
*

A knowledge of lean and/or six sigma methodologies



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

At AstraZeneca, you'll find yourself part of a team where everyone feels personally connected to the impact we make. From our science labs to large-scale manufacturing, we are committed to delivering high-quality medicines that change lives. Our work is inspiring and rewarding as we influence every part of the product lifecycle to ultimately improve lives-from patients and their families to society as a whole.

Ready to make a difference? Apply with your CV and cover letter no later than October 13th, 2025 and join us on this exciting journey! Visa mindre

At AstraZeneca Sweden, you are a key part of AstraZeneca's global success. The work that you do here is highly valued and makes a direct impact to the enterprise, and to societies worldwide. In our dynamic environment, be supported by the brightest minds working together side by side. Agile and collaborative, we work cross-functionally to succeed together. This is a place of great passion and pride. Where we work hard to build successful, inclusive and diverse teams that collaborate across the enterprise and beyond. Always striving for better, where new ideas are encouraged, and failure is an anticipated part of our innovation process.

We are currently looking for a Senior HR Advisor to our HR Services Team (Advice & Guidance) in Gothenburg, Sweden, where you'll play a key role in making AstraZeneca a great place to work-empowering managers and employees to excel, and supporting an inclusive, challenge-driven, and high-performance culture.

Key Responsibilities

In this role, you'll act as a trusted advisor and HR process expert, ensuring the highest standards of service for our Swedish operations.

You will:

* Resolve HR queries for managers and employees-guiding them to interpret and apply HR policy confidently
* Ensure exceptional support quality aligned to legal requirements, internal standards, and written procedures
* Optimize our AskAZ Portal and keep AZ Knowledge Articles up-to-date
* Manage leave of absence processes (maternity, parental, sickness, etc.)
* Issue employment confirmations and certificates, including those requiring E-ID
* Support Time & Absence Management
* Help with basic HR reporting queries
* Coordinate global HR project implementations
* Connect with Centres of Excellence (CoEs) to stay abreast of policy and process changes affecting employee data
* Prioritize workload to hit unit and personal targets, continuously seeking ways to simplify and improve processes and systems

Essential Requirements

* Minimum 4 years' HR experience supporting the Swedish market
* Attention to detail and commitment to data accuracy
* Fluency in both Swedish and English
* Solid understanding of Swedish labour law
* Experience using a ticketing system
* Ability to manage competing priorities efficiently
* Strong communication and stakeholder engagement skills
* Collaborative, team-oriented approach
* Proficiency in Microsoft applications
* Ability to handle confidential data with professionalism
* Analytical thinking and a problem-solving mindset
* Flexibility and adaptability

Desirable Requirements

* Background in HR Operations or HR Services
* Familiarity with Workday, ServiceNow, or other HCMS
* Relevant HR qualification
* Experience working in a matrix environment

We believe bold thinking happens when diverse teams connect face-to-face. Our Gothenburg site blends dynamic in-person collaboration (at least three days per week in the office on average) with the flexibility to support your individual needs.

Why AstraZeneca?

Join a purpose-driven, global team powering our mission to advance science and improve patient outcomes. Every day presents new opportunities to challenge the status quo, unlock potential, and have a meaningful impact.

Ready to join us? Submit your cover letter and CV by 28 September to become part of our journey! Visa mindre

At AstraZeneca, we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges.

We recognize the unique potential of every employee and encourage you to grow beyond what you thought possible. Your skills and passion help shape our success, and we actively support you to reach new heights, wherever your journey with AstraZeneca begins.

Within our HR function, our vision is to be recognized for delivering outstanding people practices, driving business growth, and supporting employees to thrive. Through rewarding performance and continuous innovation, we work alongside the business to propel scientific progress and deliver life-changing medicines.

As part of AstraZeneca's Human Resources team, you will develop in a dynamic, entrepreneurial environment that values results-oriented and innovative thinking.

We are now offering a 13-month temporary opportunity for a Reward Specialist in Gothenburg or Södertälje. This role is perfect for someone eager to expand their expertise, take a leading role in AstraZeneca's Reward agenda for Sweden, and contribute to Reward & Inclusion initiatives at the global level.

Main Duties and Responsibilities

In this role, you will have the opportunity to develop professionally while playing a key part in shaping AstraZeneca's Reward strategy for Sweden.

Key accountabilities include:

* Stakeholder Partnership: Engage key stakeholders to offer insights and analysis supporting AZ's ability to hire and retain top talent in Sweden.
* Reward Practices & Governance: Deliver and maintain local reward policies aligned to global standards; ensure compliance with legislative changes and global governance; keep Reward Director updated.
* Union & Social Partner Negotiations: Lead salary negotiations and communicate AZ's position on reward.
* Compensation & Market Analysis: Provide compensation insights, conduct market benchmarking, and manage annual and compliance reviews-including equal pay reporting.
* Knowledge Sharing: Use global training materials to enhance reward knowledge among business leaders and HR colleagues.

Essential Requirements

Success in this role requires a proactive, can-do mindset and the ability to quickly add value. You will collaborate confidently with colleagues at all levels and act as AstraZeneca's key internal consultant on all matters related to Reward. The ideal candidate offers:

* Expertise in Compensation & Benefits: Comprehensive understanding of reward practices, able to advise senior HR and business stakeholders across Sweden.
* Multinational Experience: Solid background in delivering compensation solutions within large, complex organisations.
* Education: University degree or equivalent.
* Supplier Relationship Management: Proven experience overseeing contracts and third-party partners.
* Interpersonal & Negotiation Skills: Exceptional relationship-building and negotiation abilities with internal teams and external partners.
* Technical Proficiency: Experience with HRIS systems is helpful, though not required.

Why Join Us?

At AstraZeneca, learning and diversity fuel our growth and success. We work inclusively across all functions, applying creativity to every challenge and supporting each other to achieve our best. With exceptional opportunity for career development, this is the ideal place to build your reputation and make a lasting impact.

So, what's next?

If you're excited by the opportunity to join us, we look forward to receiving your application. Applications are being reviewed continuously, so please submit your cover letter and CV by 23rd of September. Visa mindre

At AstraZeneca, we are committed to leading the way in turning scientific innovations into medicines that transform lives.



Pharmaceutical Technology and Development (PT&D) is the organization that turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines and providing expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.



Our Digital Science team, a part of Pharmaceutical Technology and Development, is at the forefront of digital strategy and innovation. We are seeking an Associate Principal Scientist with expertise process modeling and an interest in model governance to join our strategic global team.



Responsibilities
In this dual-focused role, you will combine your expertise in process modeling with model governance to ensure that our modeling frameworks meet the required quality standards. You will work with project teams, process engineers, mathematicians, chemists, pharmacists, materials and data scientists as well as analytical and artificial intelligence experts, to ensure that models are being correctly applied in drug projects.



Your responsibilities include:

* Supporting development and deployment of modeling and simulation tools and championing digital transformation by integrating advanced modeling tools and governance practices.
* Overseeing model lifecycle management to ensure models are maintained, updated, and retired in accordance with evolving business needs and compliance standards.
* Supporting the development and implementation of model governance frameworks to ensure consistency with internal and external quality standards.
* Collaborating with subject matter experts and cross-functional teams to establish best practices for governance protocols, adopt governance protocols and providing necessary support for implementation.
* Designing and delivering training programs to equip model developers and users with the understanding and practical skills for implementing model governance frameworks effectively.
* Keeping abreast with global developments in your area by attending conferences, workshops, webinars and being an active member of relevant networks and working groups.



Essential Requirements

* A robust scientific background with a PhD or MSc or equivalent experience in chemical engineering, physics, mathematics or related subject area.
* Experience in developing mechanistic modeling and simulation tools for problem solving and deploying those to a wider community of users.
* Skills in programming or scripting languages such as Python or Matlab for developing modeling solutions.
* Understanding and interest in developing and implementing standards and governance frameworks that ensure model quality and consistency.
* Excellent interpersonal and communication skills, with a proven ability to collaborate with cross-functional teams
* Cultural awareness



Desirable Requirements

* Understanding of regulatory standards related to model governance in the pharmaceutical or other regulated industry and experience in model governance.
* Familiarity with advanced simulation tools like gPROMS, Aspen, or ANSYS Fluent/CFX and their application in process modeling.



At AstraZeneca, we're dedicated to being a Great Place to Work. We are united by our shared purpose - to push the boundaries of science to deliver life-changing medicines. We come to work each day to make a difference - to patients, society, and our company. Our workforce reflects the people we serve - diversity is embedded in everything we do. We're at our best when drawing on our different views, experiences, and strengths. We are forever connecting, collaborating, innovating, and learning.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. We balance the expectation of being in the office while respecting individual flexibility.



Join us in this exciting opportunity! Apply with your CV and cover letter no later than September 8th 2025. Visa mindre

Introduction to role:

Are you ready to make a significant impact in the world of pharmaceuticals? We have a great opportunity for an Associate Principal Packaging Engineer within our Pharmaceutical Technology and Development (PT&D) department. This role is pivotal in supporting our entire PT&D product and packaging portfolio, transforming groundbreaking science into medicines that improve lives. PT&D spans the entire value chain, providing essential ingredients, formulations, and devices for new medicines, from early toxicology studies to clinical trials and scaling up drug production.



Accountabilities:

As an Associate Principal Packaging Engineer, you will lead packaging development across our diverse product portfolio, with a focus on Oral Solid Dose packaging. Your expertise will be crucial in areas such as pharmaceutics, analytical sciences, validation science knowledge management, product robustness, analytics, process engineering, and technology enablement. Collaborating closely with our packing partners in commercial operations, you will drive sustainability, design methodology, and standardization. You will also play a key role in delivering our packaging strategy in a dynamic, multi-skilled environment.



Key responsibilities include:

*

Leading packaging support to our clinical and development product portfolio, applying specialist knowledge and expertise to achieve project targets in a timely fashion and to agreed quality standards
*

Leading multi-functional packaging projects across AstraZeneca and partner organisations and being the point of contact to technically assess proposed pack changes and influence decision making.
*

Ensuring that work is performed in accordance with appropriate safety (SHE), quality and compliance standards, e.g. GMP, and having the ability to understand and interpret packaging regulations.
*

Generating and reviewing regulatory submission documents, project plans, protocols and technical reports ensuring that the project objectives are met
*

Use your technical expertise to support our packaging strategy in materials sourcing, asset transfers, capacity expansion, and manage the packaging product lifecycle with lean and six sigma methodologies.
*

Provide leadership in the implementation of digital tools into the packaging development process



Essential Skills/Experience:

*

Bachelor's degree or equivalent experience in engineering, (Packaging or Mechanical Engineering preferred) or closely related field
*

Able to demonstrate understanding of the principles and concepts in relation to pharmaceutical packaging
*

Is a recognised leader with direct experience and project management in an array of packaging aspects in one or more of the following: materials and polymer science, design methodology, sustainability, pharmaceutical packaging regulations and testing requirements, qualification and validation of new materials, product technical transfer and patient focussed packaging.
*

Has a working understanding and experience of one or more of the following: AutoCAD, SolidWorks, computer aided engineering (FEA, Computational / conversational fluid dynamics), product data management, rapid prototyping.
*

Demonstrated ability to lead multi-functional teams across a global platform working with internal and external partners including contract manufacturers, vendors and academia while being able to hold a large degree of independence representing own department or area of expertise
*

Experience of working with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. Good Manufacturing Practice (GMP)
*

A knowledge of lean and/or six sigma methodologies



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



At AstraZeneca, you'll find yourself part of a team where everyone feels personally connected to the impact we make. From our science labs to large-scale manufacturing, we are committed to delivering high-quality medicines that change lives. Our work is inspiring and rewarding as we influence every part of the product lifecycle to ultimately improve lives-from patients and their families to society as a whole.



Ready to make a difference? Apply with your CV and cover letter no later than July 23rd 2025 and join us on this exciting journey! Visa mindre

We have a great opportunity for an Associate Principal Process Engineer to strengthen our team! In this role you will work within Technical Operations Science and Innovation (TOSI), a key function of our Pharmaceutical Technology & Development (PT&D) organization.



The PT&D Organization, within AstraZeneca Operations, is responsible for drug product design, development and technical support for drug substance and products throughout the lifecycle.



TOSI is a multi-skilled Global organization provide the expert technical support for AstraZeneca commercial small molecule drug products, product robustness, manufacturing technology strategy and Packaging Development & Technology.

Underpinning the excellent technical support that drives robust product supply are technical processes & strategies around knowledge management, manufacturability, technical validation approaches, problem solving in alignment with the delivery of the technical inputs needed for fulfilling the Global Product Supply Strategy. We work closely with many technical functions across Operations providing the ability to drive science and build capability within our organisation and our ways of working.



In Operations, we have a big ambition - to deliver more medicines to patients, quicker and more affordably. Now, more than ever, we're progressing. Using leading-edge science and digital technologies, we're driving automation and efficiency. Our vision of the 'Smart Factory' showcases us at our best. Disciplined problem solvers and doers, we thrive in our often intense and ambiguous environment, seeking out new challenges and working towards new solutions. A place where anyone is supported to step up and lead, and everyone has the freedom to take ownership and drive outcomes forward.



At AstraZeneca, we believe in the potential of our people and you'll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.



Key Accountabilities

The role of the Associate Principal Process Engineer has the following responsibilities:

* Serve as a key expert in pharmaceutical unit operations with a focus on the mechanistic understanding of process-equipment interface, providing advanced technical leadership and support.
* Apply process engineering principles to identify, develop and use modelling and simulation tools for predicting process performance, resolving operational issues, and optimising both equipment function and system integration.
* Provide technical leadership and expertise in resolving complex process-related manufacturing issues, utilising core engineering modelling and simulation to resolve complex manufacturing challenges and enhance process efficiency.
* Contribute to product supply strategy projects, including sourcing, asset transfers, capacity expansions, and the introduction of new equipment.
* Lead technical support for the transfer of established product manufacturing processes within internal manufacturing sites and to external partners, employing scale-up modelling, equipment selection, and comprehensive manufacturing engineering support.
* Propose and implement physical characterisation studies for raw materials, intermediates, and finished products to support investigations and drive improvements in formulation and manufacturing processes.
* Identify opportunities for manufacturing improvement, lead impact assessments, and support the implementation of technical improvements or major change initiatives with a focus on maintaining product performance, including contributions to regulatory file authoring, license renewals, and responses to regulatory queries, supported by model-based risk assessments.
* Drive the standardisation and modernisation of manufacturing equipment and processes across Operations, using advanced modelling and simulation to meet regulatory requirements, support good business practices, and ensure manufacturability and quality standards.



Essential requirements

* Demonstrate an understanding of the overall drug development and commercialization process from development, launch, and through life-cycle management.
* Process/chemical Engineering BSc/MSc with a few years of relevant pharmaceutical industry experience post degree or PhD level with work experience post degree
* Demonstrate an understanding of a range of unit processes and equipment for OSD manufacturing (e.g. mixing, drying, compression, roller compaction, continuous direct compression, coating) and awareness of physical characterisation of raw material, intermediate and final products (e.g. mechanical testing, particle size distribution, imaging etc).
* Experience in process scale up, manufacturing engineering and digital twins/modelling
* Experience in data analysis/data science languages and the use of digital tools.
* Experience with a range of CMC elements related to commercial product manufacturing process requirements - e.g., process establishment, optimisation and validation, control of drug products, stability, packaging and commercial manufacturing, with good understanding of SHE and cGMP.
* Experience in Pharmaceutical Operations and/or R&D with a track record of successful project leadership and delivery within a matrix organisation.
* Evidence of good communication and relationship skills.



Desirable requirements

* Experience in or exposure to multiple subject areas in CMC and related functions (e.g. Product Development, Operations, Global Supply, Marketing Companies)
* Have previous experience and training in Lean and Six Sigma, problem solving tools.
* Have experience in physical testing techniques of raw materials, intermediate and final drug products.
* Experience in or exposure to coding and programming languages.





Are you ready to bring new ideas and fresh thinking to the table? Excellent!

Please apply with your CV and cover letter. We welcome your application no later than September 4th, 2025! Visa mindre

At AstraZeneca, we unlock the power of what science can do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. With an unwavering belief in following the science we unleash our curiosity, investing in key areas, harnessing innovative technologies and taking smart risks. Help to shape the future of healthcare as we take our pipeline from strength to strength!

Business area

To meet patients' needs, AstraZeneca recognises the opportunity to apply a diverse range of new modality technologies to design novel therapeutics. This is exemplified by the increased number of new modalities entering clinical development. The Global Product Development (GPD) department has accountability for developing the pipeline of both new modality projects and traditional synthetic molecules and covers oral, parenteral and pulmonary delivery routes. It also hosts specialised Biopharmaceutics capabilities that support the whole late-stage synthetic portfolio.

GPD sits within the Pharmaceutical Technology and Development (PT&D) function. PT&D are the bridge which turns brilliant science into effective medicines that help millions of people. We work across the entire value chain, designing and delivering the active ingredients, formulations and devices required to support new and existing medicines that help millions of people.



The role

We are looking for a specialist in Physiologically Based Biopharmaceutics Models (PBBM) to join our biopharmaceutics group in Global Product Development, at the Senior Scientist level. The role can be based at either of our sites in Gothenburg, Sweden or Macclesfield, UK.

In GPD, you will be a key member of a group responsible for generating deep Biopharmaceutics understanding of drug products including conventional dosage forms, enabling formulations, nanomedicines and advanced drug delivery technologies across oral, parenteral and pulmonary delivery routes. We will rely on you to provide expertise in PBBM in order to build mechanistic understanding of drug product performance, influence product design and predict bridging study outcomes. The resulting insights will be used to guide product development teams from the early clinical phase through commercial filings and beyond to marketed products.

You will work collaboratively across boundaries at a global level to achieve these goals with team members from multiple skill areas (e.g. analytical, material science, engineering, formulation, packing and devices, clinical, supply chain and many more).

Typical responsibilities for the successful applicant will include:

* Development, validation and application of Physiologically Based Biopharmaceutics Models and other in-silico data packages to required quality and time.
* Ensuring design and development of robust products and manufacturing processes as well as support bridging and control strategies, marketing applications and downstream commercialisation activities.
* Building, documenting and clearly communicating Biopharmaceutics knowledge for assigned drug products.
* Working effectively with colleagues across Product Development, Pharmaceutical Sciences and Operations to ensure the successful delivery of drug projects spanning all phases of development, representing the biopharmaceutics skill area in project teams.
* Authoring of regulatory documentation to support clinical trial and marketing applications and ensure continued and safe access of our products to patients.
* Collaborating within the skill area to develop Biopharmaceutics technology strategies and deliver capability build activities.
* Providing technical supervision and mentoring to peers and students.
* Driving innovation, securing intellectual property and enhancing AstraZeneca's scientific reputation by publishing high calibre research and engaging in external collaborations.



Essential requirements

* Degree, preferable PhD, in a relevant subject leading to industrial or academic experience of applying Biopharmaceutics knowledge to pharmaceutical problems.
* Expert in using Physiologically based Biopharmaceutics Modelling (PBBM) software, e.g. GastroPlus, Simcyp or PK-Sim to support formulation development.
* Strong modelling skills and a proven track record of generating impactful in-silico data.
* Good understanding of the relationship between in-vitro drug product properties and in-vivo pharmacokinetic performance, ideally with knowledge of the link to control strategy development.
* Strong collaborative working and communication skills, including the ability to work effectively with colleagues from diverse backgrounds and skill areas.
* Excellent organisational and planning skills with a track record of delivering to the agreed time and quality.



Depending on the ability and experience of the successful applicant, coaching and training will be provided to ensure optimal delivery against the role.



At AstraZeneca, we 're dedicated to being a Great Place to Work, where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. We have an inclusive culture that fosters diversity and collaboration and are committed to lifelong learning, growth and development.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



Are you ready to bring new ideas and fresh thinking to the table? Excellent!

Please apply with your CV and cover letter in one document, clearly stating your Biopharmaceutics knowledge.



We welcome your application no later than August 31st, 2025! Visa mindre

Are you a driven Data Scientist with a robust foundation in traditional data science methods and a passion for Agentic AI, and human-in-the-loop (HITL) multi-agent systems? If so, an exciting opportunity awaits you at AstraZeneca!



We are looking for Associate Principal AI Data Scientists eager to utilize their expertise in these advanced technologies to revolutionise our drug development processes. In the Pharmaceutical Technology and Development (PT&D) department, you will be a key player in transforming molecules into groundbreaking medical treatments. PT&D leads the charge in developing cutting-edge synthetic routes, drug formulations and delivery technologies, ensuring our products are effective, safe, and of the highest quality.



Your role involves contributing data science expertise into cross functional global pharmaceutical development projects in support of transforming the way we deliver medicines to patients. You'll play a pivotal role in shaping our AI strategy and driving the co-development of sophisticated HITL multi-agent systems.

This is an individual contributor role and will be based at our dynamic sites in Gothenburg (Sweden) or Macclesfield (UK).



Accountabilities:

*

Drive innovation in agentic AI, multi-agent systems, and digital twins, exploring new methodologies and applications.

*

Design, implement, and optimize algorithms for autonomous decision-making, coordination, and policy learning among agents and digital twins.

*

Evaluate agent performance in the context of decision making, collaboration, competition, uncertainty.

*

Drive machine learning initiatives focused on applications within drug development projects.

*

Collaborate with cross-functional teams ensuring knowledge transfer to IT engineering teams for IT solution builds and deployment.

*

Keep pace with industry advancements by reviewing academic papers and attending conferences. Publish findings in peer-reviewed journals and represent the company at scientific forums.

*

Communicate technical concepts and results to technical and non-technical audiences.



Essential skills/Experience:

*

Advanced degree in computer science, data science, artificial intelligence, machine learning or related fields.

*

Excellent coding skills in languages such as Python, R.

*

Hands-on industrial experience designing multi-agent patterns, digital twins and experience with agentic AI design patterns, reinforcement learning.

*

Extensive industrial experience with AI and ML frameworks like TensorFlow, PyTorch,

*

Hands-on experience with GenAI orchestration frameworks such as LangGraph, CrewAI.

*

Hands-on industrial experience with applied machine learning domains such as deep learning, causal machine learning, transfer learning.



Desirable skills/experience:

*

Contributions to open-source projects. If you meet these criteria, please highlight merged GitHub PRs in your application.

*

Strong publication record in the field of AI.

*

Experience designing multi-agent systems in the pharmaceutical sector.

*

Experience delivering machine learning projects with applications in pharmaceutical development, chemical engineering or chemistry.

*

Experience with one or more of the following applied machine learning domains such as federated learning, few/zero shot learning, meta learning, explainable AI.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



AstraZeneca is a place where change is embraced, and new solutions are trialled with patients and business in mind. Here, technology is a key lever for delivering medicines quickly, affordably, and sustainably. Our diverse workforce is united by curiosity, sharing learnings to scale fast. Be part of a digitally-enabled environment that impacts all parts of the business-from robotic process automation to machine learning for quality batches-while contributing to society and the planet.



Ready to make a difference? Apply now to join our team!

Welcome with your application no later than August 28th 2025.



Competitive salary and benefits package on offer.

Opening date: August 14th, 2025
Closing date: August 28th, 2025 Visa mindre

Are you passionate about transforming science into clear and compelling regulatory documents that drive successful drug development? We are seeking a talented and experienced Associate Director, Clinical Regulatory Writing to join our CVRM (Cardiovascular, Renal, Metabolic) Clinical Regulatory Writing team in Gothenburg, Sweden. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work- where the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

About AstraZeneca

AstraZeneca is a global, science-led biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that transform lives. Operating in over 100 countries and supported by a robust pipeline, our work addresses some of the world's most serious illnesses across oncology, cardiovascular, renal, metabolism, respiratory, and immunology. Driven by our values and innovation-led culture, we are focused on making a meaningful difference to patients, healthcare systems, and society as a whole.



About the Role

The CVRM Clinical Regulatory Writing group provides expert strategic leadership and communications expertise to clinical drug programs, ensuring delivery of high-quality, label-focused documents aligned with project strategy, regulatory requirements, and communications best practices. Role holders not only author critical clinical-regulatory documents but also act as critical reviewers to achieve the highest quality standards. Team members also represent the Clinical Regulatory Writing skill set on both drug and non-drug projects, advocating for best practices and continuous improvement.



Key Responsibilities

As an Associate Director, Clinical Regulatory Writing, you will:

* Provide strategic leadership and communication expertise to clinical drug programs across the CVRM portfolio.
* Author and critically review clinical-regulatory documents, ensuring the highest regulatory, technical, and quality standards.
* Represent Clinical Regulatory Writing on project teams, advocating for communication best practices.
* Provide strategic communications leadership within clinical delivery or submission teams, establishing standards and promoting quality and efficiency.
* Act as submission lead, driving development of the clinical Submission Communication Strategy (cSCS).
* Lead both internal and external authoring teams and cultivate strong partnerships with vendor medical writers to ensure timely, high-quality document delivery.
* Translate complex clinical data into clear, concise, and accurate messages tailored to specific audiences.
* Serve as a strategic thinker who can conduct high-level document reviews.
* Collaborate proactively with other functions at the program level.
* Support the development and upskilling of colleagues within the Clinical Regulatory Writing function.
* Champion continuous improvement and operational excellence in communications.



Essential Requirements

* Bachelor's degree in Life Sciences or a related discipline.
* Significant medical writing experience within the pharmaceutical industry or a Contract Research Organization (CRO).
* Proven ability to advise and lead communications projects and teams.
* Strong understanding of drug development and the communications process from early development through to launch and lifecycle management.
* In-depth knowledge of technical and regulatory requirements relevant to clinical regulatory writing.



Desirable Qualifications

* Advanced degree in a scientific discipline (e.g., Ph.D.).



If you are driven to deliver impactful regulatory communications, excel in multidisciplinary teams, and want to shape the future of clinical development, we encourage you to apply.



Apply with your cover letter and CV by 24 August!



Explore more about:

Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Inclusion & Diversity at AstraZeneca: https://careers.astrazeneca.com/inclusion-diversity

Sustainability at AstraZeneca: https://www.astrazeneca.com/sustainability/resources.html Visa mindre

Are you a scientist or engineer passionate about transforming drug discovery through cutting-edge molecular simulations and artificial intelligence? Are you driven by the opportunity to help develop life-changing medicines? If you have recently completed your PhD or have a few years of postdoctoral experience and are eager to take the next step in your career, this is an exciting chance to join the innovative Molecular AI department at AstraZeneca in Gothenburg, Sweden.

Our vibrant Gothenburg site is home to more than 2,400 employees from over 50 countries, creating an inspiring and collaborative environment where diverse perspectives and scientific breakthroughs drive new discoveries. We believe the diversity of our team is critical to turning bold ideas into reality. To foster this collaborative spirit, we expect all team members to work on-site at least three days per week.

At AstraZeneca, your engineering expertise and enthusiasm will directly impact our technology platforms and shape the future of transformative medicines. Are you ready to make a difference? Join us and be part of our journey.



What You'll Do

As a Scientific Software Developer, you will have a profound impact on multiple projects across AstraZeneca, with a focus on software development and applying molecular simulations to the discovery of new drugs. You will:

*

Develop software and complex workflows for molecular simulations-from molecular dynamics to quantum mechanical calculations.

*

Enhance and maintain MAIZE, our workflow manager (see more on GitHub).

*

Apply advanced simulation methods to drive real-world drug discovery projects.

*

Collaborate closely with computational & medicinal chemists to capture user requirements.

*

Work with IT engineers to deliver robust workflows and software to users.

*

Contribute to open-source initiatives and the broader computational chemistry community.

*

Actively mentor our cohort of postdocs, PhD, and Master students.



Essential Qualifications

We believe you are passionate about building software solutions for life sciences. You have:

*

A PhD in chemistry, physics, computer science, or related field, or equivalent experience gained in an industrial setting.

*

Deep expertise and practical experience in molecular simulations, evidenced by peer-reviewed publications or impactful project outcomes.

*

Excellent programming skills, preferably in Python. Experience in contributing to open-source projects is highly desirable.

*

Exceptional written and verbal communication abilities, with a proven track record of explaining complex technical concepts clearly to a variety of audiences.

*

Proven ability to work inclusively within multidisciplinary teams, with a focus on building a positive and collaborative team culture.



Desirable Requirements

You would benefit from having experience or familiarity with:

*

Collaborative software development practices such as version control and code review.

*

Crafting and developing robust, reproducible, and extensible software solutions.

*

Understanding of advanced software concepts, including concurrency, sockets, interprocess communication, and serialization.

*

Experience with high-performance computing environments, such as clusters or cloud-based solutions.

*

Proficiency in quantum chemistry and molecular docking software.

*

Practical experience of machine learning or artificial intelligence

*

Ambition to supervise Master Thesis students, Graduate students PhD students.



Why AstraZeneca?

At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.



So, what's next?

Ready to make a difference? Apply now with your CV and cover letter, no later than 17th of August!



For more information regarding the role, please contact: Samuel Genheden [email protected]



Explore more about:

Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Inclusion & Diversity at AstraZeneca: https://careers.astrazeneca.com/inclusion-diversity

Sustainability at AstraZeneca: https://www.astrazeneca.com/sustainability/resources.html Visa mindre

Are you a scientist with expertise in analytical chemistry and automation? Would you like to work in an environment using state of the art technology in a company that follows the science and turns ideas into life changing medicines? Then we have an opportunity for you!



The Role

We are seeking a Senior Scientist to join our Separation Science Laboratory, where you will help drive analytical and purification excellence within our R&D organization. In this hands-on laboratory role, you will apply your chromatography expertise to deliver pure, well-characterized compounds that will enable scientific advancement across diverse projects. You will work collaboratively with colleagues, address complex technical challenges, and develop innovative solutions to propel project objectives at various stages of drug discovery.

At the Senior Scientist level, you will be expected to lead local scientific and technological development projects and contribute to global initiatives, ensuring our separation science capabilities continue to meet future demands. Based at AstraZeneca's vibrant R&D site in Gothenburg, Sweden, this role offers a unique opportunity to combine practical laboratory skills with deep theoretical knowledge and make a meaningful impact within a vibrant scientific community.



Pharmaceutical Sciences is a function within AstraZeneca's Biopharmaceuticals R&D unit that creates innovative, efficient solutions by transforming molecules into investigative medicines meeting the unmet needs of future patients. The function has five departments: Early Chemical Development, Advanced Drug Delivery, Early Product Development and Manufacturing, Project Management, and Data Science and Modelling. Our multifaceted portfolio of projects includes traditional small molecules, nucleotide-based therapies, and nanomedicines across AstraZeneca's therapy areas.

Early Chemical Development is responsible for developing manufacturing routes and processes as well as delivering batches of drug substance for projects in the late discovery and early development portfolio and its key skill areas include Analytical Chemistry, Crystallization, Isotope Chemistry, Large-Scale Laboratory (Kilo-Lab) Manufacturing, Process Chemistry, Process Engineering and Separation Science.

The Separation Science Laboratory supports the design and evaluation of new candidate drugs through purification and characterization of small molecules and New Modalities. Our state-of-the-art laboratories are equipped with a comprehensive range of chromatography systems to support various scales (mg to kg), complemented by a wide array of detectors and liquid handling technologies. This cutting-edge infrastructure enables us to efficiently support projects throughout the drug discovery process.



Education, Qualifications, Skills, and Experience

*

A Ph.D. in Analytical Chemistry or a related field or a university degree with at least 3 years relevant postgraduate experience
*

Excellent knowledge of analytical chromatographic and detection techniques, including method development and instrument troubleshooting
*

A track record of applying analytical chemistry techniques to solve scientific problems
*

Proven laboratory skills and a strong desire to contribute practically
*

Excellent collaboration, communication, and planning skills with a strong sense of responsibility, teamwork, and delivery focus
*

Experience in developing scripts to support laboratory automation workflows is highly desirable, with expertise in Python or other relevant automation programming languages preferred.



If your passion is science and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be.



What's next?

Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours.

If you are interested, apply now!

Please note applications must include your CV and a cover letter which presents you and your key areas of strength / development and why you should be considered for the role (Please make sure to combine your cover letter and CV into a single document, as the system only allows you to upload one file).



Welcome with your application no later than 17th August 2025. Visa mindre

At AstraZeneca, Scientific Computing is a strategic asset underpinning our advances in science. Our research into disease and creating new medicines critically depends on continuously developing and refining best-in-class computing capabilities and the engineering teams supporting them.

We are looking for a highly motivated individual to lead HPC Infrastructure as part of our platform leadership team. If you combine excitement for HPC technology with a passion for science, and an understanding of balancing agile innovation with providing an enterprise-quality service, then we want to hear from you

The Scientific Computing platform (SCP) is AstraZeneca's primary platform supporting exploratory research, and underpins every stage of drug development from target validation through to compound selection for clinical trials. At its heart it provides some key capabilities:

*

HPC clusters on-prem, in the cloud and through external partnerships

*

Applications and software packages the scientists need to perform their research

*

Expertise to help scientists optimise their workflows and accelerate the development of new medical treatments.



A critical ability is to maintain the flexibility to adjust and adapt according to changing requirements and follow the science.

The SCP department comprises 50-60 individuals across three core technical areas (HPC Infrastructure, Software Infrastructure, and Applications), a Business Engagement team, an Operations team, and a small Program Management team.

About this role

As the HPC Infrastructure Technical Lead, you will be leading a team of 10-15 engineers and be engaged in a variety of activities including responsibility for

*

Working with scientific users to understand their needs, and develop solutions

*

Horizon scanning, identifying the future technologies needed to stay innovative

*

Defining the roadmap for the platform's HPC infrastructure

*

Prioritising the work backlog for the team according to scientific needs

*

Ensuring delivery of team objectives, both for on-premises clusters and in the cloud

*

Mentoring and coaching engineers

*

Investigating and resolving complex operational incidents

*

Ensuring the timely adoption of cloud services for all of SCP's needs

Essential Skills

*

Experience leading the engineering for large-scale computing environments, such as HPC, HTC for scientific research, preferably in Life Sciences (e.g. Pharmaceutical Industry, BioTech)

*

You can demonstrate a deep understanding of HPC architectures and the factors influencing their performance , including:

*

Processor and accelerator architectures

*

HPC high performance network technologies, such as Infiniband, low latency ethernet at 100Gbit and above

*

High performance storage systems (e.g. GPFS, Lustre, Weka)

*

Strong understanding of HPC scheduling systems (e.g. SLURM, LSF)

*

Strong communication skills, with the ability to explain complex technical topics to non-experts, and interpret scientific needs in terms of IT

*

Operation and configuration of public cloud computing infrastructure (e.g. AWS, Azure, GCP), especially in an HPC context

*

Experience working with distributed DevOps teams using agile methods, and using other project management techniques when appropriate

Desired Skills & Background

*

Experience optimising HPC inftastructure for applications commonly used in drug discovery; e.g. molecular dynamics, genomics and machine learning

*

Experience deploying and operating OpenStack

*

Experience with a variety of programming languages and frameworks, used in research computing and AI (MPI, C/C++, CUDA, Pytorch/Tensorflow, Python/conda, R)

*

You will have a bachelor's degree or higher in Computational, Physical or Biological Science, Engineering or equivalent area



So, what's next!

If you are interested, apply now but no later than July 31st. Due to summer Holidays you may not hear from us until mid-August.



About AstraZeneca

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for the world's most serious diseases. AstraZeneca is one of only a handful of pure-play biopharmaceutical companies to span the entire value chain of a medicine from discovery, early- and late-stage development to manufacturing and distribution, and the global commercialization of primary care, specialty care-led and specialty care medicines that transform lives.

Our primary focus is on three key areas of healthcare: Cardiovascular and Metabolic disease (CVMD); Oncology; and Respiratory, Inflammation and Autoimmunity (RIA). We are also active in the Infection, Neuroscience and Gastrointestinal (ING) disease areas.

AstraZeneca is committed to promoting a healthy work-life balance, and this role is a hybrid role allowing flexible working, 60% in the office. Visa mindre

At AstraZeneca, we are an equal opportunity employer that puts patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, a team leader, thinking big and working together to make the impossible a reality.



As part of the Global Human Resources team at AstraZeneca, you will have the opportunity to thrive in a fast-paced, creative and purposeful environment where bold, innovative thinking is encouraged. We believe our people are our greatest asset and are always looking for top talent whose curiosity, learning-agility and strong values orientation results in the delivery of high quality, impactful outcomes that accelerate our people and business success.



We are seeking an HR Solutions Partner for a 12-month contract to support our Operations and IT divisions. In this role, you will work closely with HR Business Partners and HR Centres of Expertise (CoE) to deliver high-quality HR support to leaders and employees. Reporting to an HR Solutions Manager who oversees a global team of HR Solutions Partners, you will be based at our Gothenburg site-a vibrant hub of innovation, home to over 2,400 colleagues from more than 50 countries. Here, diversity is celebrated as a key driver of creativity, scientific progress, and meaningful change for patients across the globe.



As an HR Solutions Partner, you will collaborate with HRBPs to provide expert guidance and coaching to managers and HR colleagues on all HR policies, processes, and programmes. You will play an important role in supporting business-specific HR initiatives in a fast-paced and evolving environment, helping to shape the future of AstraZeneca.



If you are motivated by challenge, inspired by change, and committed to making a real-world impact, we encourage you to apply and join us on our journey to push the boundaries of science and talent development.



Main Duties & Responsibilities:

* Provide generalist HR advice on a range of employment related matters (e.g., disciplinary and grievance cases, attendance management, parental leave) and escalate to Employee Relations Specialist or COEs as appropriate
* Work collaboratively with colleagues located in Global and Regional HR Center and HR Services teams in other countries to improve the customer experience, through accuracy and pace of delivery
* Deliver sound generalist HR support, acting as a key point-of-contact and a trusted partner for provision of professional advice and support to a range of HR activities and programs
* Ensure flawless execution of key people processes across the business - leading and supporting HRBP's with Performance Management, Reward, Employee Relations, change management, compensation and Workforce Planning processes
* Co-design, lead and drive key HR project delivery within the BBU, in line with defined People Plan priorities, with support, coaching and guidance from the HRBPs
* Deputise for HRBPs on key meetings and functional communication activity, where necessary
* Maintain a high level of communication with all levels of the organization (both globally and locally) and positively impact the key decisions



Essential Requirements:

* Relevant HR experience
* 0-2 years of HR experience
* Bachelor's Degree
* Practical experience providing HR advice to colleagues and senior leaders
* Excellent analytical skills
* Technical HR knowledge / skills associated one or more of the following disciplines - Resourcing, Performance & Reward, Employee Relations, L&D, organisational change
* Attention to detail; accomplishes tasks and processes accurately and completely
* Effective communicator and able to build relationships quickly
* Self-starter, being able to deliver on own initiative and prioritise independently
* Hunger for personal learning and self-driven development
* Proven project management capability
* Demonstrated ability to use Microsoft Office products is required (Word, Excel, Outlook, PowerPoint, Box)



Desirable requirements:

* Possesses knowledge and understanding of HR systems (Workday, ServiceNow)
* Experience in managing / interacting with sizeable internal customer base
* General knowledge and understanding of AZ policies and procedures



Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us while we continue to build a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we are developing new ways to work, ground breaking methods, and bringing unexpected teams together. Interested? Come and join our team!



So, what's next?

Ready to make a difference? We will be reviewing applications ongoing, so apply now with your CV and cover letter, no later than 24th of July!



Explore more about:

Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Inclusion & Diversity at AstraZeneca: https://careers.astrazeneca.com/inclusion-diversity

Sustainability at AstraZeneca: https://www.astrazeneca.com/sustainability/resources.html Visa mindre

Do you have a statistical expertise and in-depth knowledge within pharma or healthcare? Would you like to combine your leadership skills with your understanding of the technical and regulatory requirements of drug development in a global company that follows the science and turns ideas into life changing medicines? Join us then at AstraZeneca to develop the future treatments of Respiratory and Immunology (R&I) diseases!

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

We now offer an exciting opportunity for a Biometric Team Lead with passion, expertise, and experience in developing, coaching, and mentoring a team of fantastic statisticians.

The role will be based in Gothenburg SE.

What you'll do

The Biometrics Team Lead is responsible for the biometrics contribution in one or more drug projects across all phases of development and is line managing a group of statisticians. You will have 6 -10 statisticians directly reporting to you.



Major Responsibilities

In the role, you will:

* Lead the strategic and operational planning of the Late R&I Biometrics contributions, to the Development Plans, Regulatory Strategy and Submissions, Health Technology Assessment and Commercial support of AZ products
* Provide leadership for Biometrics staff world-wide so that all work is carried out with regards to AstraZeneca standards and external regulations
* Performance management of your direct reports
* Coach your direct reports to rapid professional development
* Provide leadership and direction to improvement projects/activities/initiatives and drive the implementation of best practice across the department
* Together with your team lead colleagues secure biometrics contribution to the whole Late R&I development portfolio
* Represent AstraZeneca to Health Authorities and Reimbursement/Payer organizations
* Investigate and implement statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration
* Develop contacts with international opinion leaders, consultants and collaborative groups Organizations



Essential for the role

* MSc/PhD in Statistics or Mathematics -containing a substantial statistical component
* Experience in line management and/or project management
* In depth knowledge of the technical and regulatory requirements related to the role of statistician in drug development
* Extensive experience of drug development, program design, data analysis and interpretation
* Experience of regulatory interactions and/or submissions
* In order to be successful in the role as Biometric Team Lead in our organization, we believe that you are a skilled communicator and that you have an excellent ability to build strong relationships. You are also a talented collaborator in order to work across global & functional boundaries, both internally and externally.



So, what's next?

Are you already imagining yourself joining us? Good, because we can't wait to hear from you! Welcome with your application (CV and cover letter) no later than July 20, 2025.

We will review the applications continuously so please apply as soon as possible.

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity, no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey. Visa mindre

HPC engineer Embark on a significant journey where your expertise in high-performance computing accelerates scientific discovery and impacts patient outcomes worldwide.

We are currently seeking a passionate, HPC engineer to join AstraZeneca's vibrant site in Gothenburg, Sweden. The ideal candidate will have extensive hands-on experience making an impact with HPC technology, delivering HPC services to a high quality, and able to relate to the scientific community and work closely with users to make the best use of research computing services.

About the Role:

At AstraZeneca, our Research Data & Analytics Team is at the cutting edge of transforming how we discover and develop medicine. As an HPC Engineer within the Scientific Computing Platform, you'll be crucial in delivering HPC services and solutions that drive progress in computational chemistry, imaging, multi-OMICs, AI and more. We're combining modern HPC with leading DevOps and cloud-native technologies to push the boundaries of biopharmaceutical research.

The HPC landscape is continually evolving. You will need the skills to help build and operate industry-leading capabilities, including application build frameworks, containerized applications and cloud software-as-a-service. Automated deployment is a key feature and you will need to be comfortable with DevOps processes and delivering consistency through automation and infrastructure-as-code.

Your Impact:

Be part of a global team where your skills in high-performance computing empower innovative scientific solutions. Engage and collaborate with researchers and engineers to optimize workflows and deploy HPC capabilities that facilitate new discoveries. Your contribution will directly enhance the development of innovative medicines, improving patient outcomes globally.

Key Responsibilities:

*

Develop and operate cutting-edge research computing services and applications

*

Adopt Site Reliability Engineering principles to manage end-to-end HPC service operations, monitoring, and incident response

*

Optimize and solve complex technical problems in the HPC infrastructure and the cloud, collaborating closely with scientific users to enhance system utilization

What You Bring:

*

Proficiency in Linux environments for administration and programming

*

Solid skills in Python programming and bash scripting

*

Highly customer-focused, with the ability to communicate complex IT concepts to non-experts

*

Experience in working within a DevOps team using agile methodologies

*

Experience of building and operating services in the cloud

Desired Skills and Expertise:

*

Background in a scientific field or experience with computationally intensive scientific data analysis

*

Experience in large-scale HPC environments, parallel filesystems, and with tools such as SLURM and OpenStack

*

Familiarity with configuration automation, software distribution frameworks, and cloud deployment, especially AWS

*

Expertise in AI/ML tools, parallel programming, and containerization technologies

*

Understanding of domain-specific applications like bioinformatics tools, simulation software, or high-performance data visualisation packages



Join AstraZeneca and play a pivotal role in advancing HPC technology to accelerate scientific breakthroughs.

Apply now to be a leader in HPC innovation at AstraZeneca!



ABOUT ASTRAZENECA

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energised and rewarded for their ideas and creativity.



Where can I find out more?

AstraZeneca Gothenburg site: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre

Join AstraZeneca, a global, science-led, patient-focused biopharmaceutical company, as our Science & Innovation Director - AI.



This role is a unique opportunity to drive and champion the innovative application of a range of physics-informed and statistical Artificial Intelligence (AI) tools in Pharmaceutical Development. You will be at the forefront of creating new business opportunities and responding to short and long-term business needs.



Pharmaceutical Technology and Development (PT&D) is an organization within Operations that turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines. We provide the essential data that forms the core of the regulatory submission files and provide expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.



The role



PT&D is embarking on an ambitious digital strategy; recognising the potential for transformational impact on how Medicines are developed. As a Science & Innovation Director, you will be expected to keep up-to-date on how AI is developing and to use this knowledge to identify and progress opportunities where AI could have a transformational impact. You will be responsible for developing a business-focused science and innovation strategy with clear ambitions and deliverables. You will use your knowledge of AI to work collaboratively with external partners to evaluate these opportunities through the PT&D Innovation process. A strong external network will be essential for this role to understand advancements and to collaborate with external parties on innovation opportunities. In PT&D, collaboration is also key and you will be responsible for championing successful Innovation projects, acting as a change agent to ensure implementation & the transformational impact is realised.



The role holder will build a global network and high-quality links/collaborations with key academic partners, companies and other innovators and advise in the selection and design of collaborations with universities and other institutions. You will act as ambassador for creativity and innovation and facilitate wider understanding how PT&&D can influence patient value.



Essential Skills/Experience:

*

Master or PhD degree in computer science or life sciences degree
*

Demonstrated knowledge, capabilities of a range of Artificial Intelligence tools and application of these in a science-based setting.
*

A strong scientific background in the pharmaceutical industry, ideally in area of Chemistry Manufacture and Control.
*

Track record of identifying & driving innovation and implementing change
*

Demonstrated ability to collaborate and influence effectively internally and externally
*

A track record of successful leadership and delivery.
*

Experience and ability to work across several scientific areas.
*

Proven strong communication and stakeholder management skills



Desirable Skills/Experience:

*

Demonstrates a high level of understanding of the AI area and can relate this to the challenges & opportunities faced by PT&D in developing new medicines.
*

Excellent team working and networking skills.
*

Ability to think beyond boundaries of own job and company, challenges status quo and seeks opportunities for business improvement.
*

Capable of making effective decisions, acts courageously and communicates with conviction and inspiration at all levels.
*

An excellent communicator with experience of interacting effectively across interfaces of subject area, culture and expertise both internally and externally.



At AstraZeneca, we're dedicated to being a Great Place to Work. We are united by our shared purpose - to push the boundaries of science to deliver life-changing medicines. We come to work each day to make a difference - to patients, society, and our company. Our workforce reflects the people we serve - diversity is embedded in everything we do. We're at our best when drawing on our different views, experiences, and strengths. We are forever connecting, collaborating, innovating, and learning.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. We balance the expectation of being in the office while respecting individual flexibility. Please mark your application with your preferred work location (Gothenburg or Macclesfield)



Join us in this exciting opportunity! Apply with your CV and cover letter no later than July 23rd 2025. .



Competitive salary and benefits package on offer.

Opening date: July 2nd, 2025
Closing date: July 23rd, 2025 Visa mindre

Join AstraZeneca, a global, science-led, patient-focused biopharmaceutical company, as our Science & Innovation Director in Robotics!



This role is a unique opportunity to drive and champion the transformational potential of automation and robotics in Pharmaceutical Development. You will be at the forefront of creating new business opportunities responding to business needs and focussing on longer-term opportunities.



Pharmaceutical Technology and Development (PT&D) is an organization within Operations that turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing, delivering and analysing active ingredients, formulations and devices for new medicines. We provide the essential data that forms the core of the regulatory submission files and provide expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.



The role

PT&D recognises the potential for automation and robotics to have a transformational impact on how medicines are developed. As a Science & Innovation Director, you will be expected to keep up-to-date on how these rapidly evolving areas are developing and to use this knowledge to identify and progress opportunities that could impact PT&D.

*

You will be responsible for developing a business-focused science and innovation strategy with clear ambitions and deliverables.
*

You will use your knowledge of automation and robotics to work collaboratively with external partners to evaluate these opportunities through the PT&D Innovation process.
*

A strong external network will be necessary for this role, to understand advancements and to collaborate with external parties on innovation opportunities.
*

In PT&D, collaboration is key and you will be responsible for championing successful Innovation projects, acting as a change agent to ensure implementation & that the transformational impact is realised.



The role holder will build a global network and high-quality links/collaborations with key academic partners, companies and other innovators and advise in the selection and design of collaborations with universities and other institutions. You will act as ambassador for creativity and innovation and facilitate wider understanding how PT&&D can influence patient value.



Essential Skills/Experience:

*

Master or PhD degree in computer science, life sciences or engineering
*

Demonstrated depth of knowledge in the area of automation & robotics and the application of these in a science-based setting.
*

A strong scientific background or equivalent experience in the pharmaceutical industry, ideally in area of Chemistry Manufacture and Control (CMC).
*

Track record of identifying & driving transformative innovation and implementing change to achieve maximum business benefit
*

Strong external network in the area of automation & robotics with demonstrated ability to collaborate and influence effectively internally and externally
*

A track record of successful leadership and delivery.
*

Experience and ability to work across several scientific areas to a common goal.
*

Proven strong communication skills and stakeholder management



Desirable Skills/Experience:

*

Demonstrates a high level of understanding of the automation and robotics area and can relate this to the challenges & opportunities faced by PT&D in developing new medicines.
*

Excellent team working and networking skills.
*

Ability to think beyond boundaries of own job and company, challenges status quo and seeks opportunities for business improvement.
*

Capable of making effective decisions, acts courageously and communicates with conviction and inspiration at all levels.
*

An excellent communicator with experience of interacting effectively across interfaces of subject areas, culture and expertise both internally and externally.



At AstraZeneca, we're dedicated to being a Great Place to Work. We are united by our shared purpose - to push the boundaries of science to deliver life-changing medicines. We come to work each day to make a difference - to patients, society, and our company. Our workforce reflects the people we serve - diversity is embedded in everything we do.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. We balance the expectation of being in the office while respecting individual flexibility. Please mark your application with your preferred work location (Gothenburg or Macclesfield)



Join us in this exciting opportunity! Apply with your CV and cover letter no later than July 30th 2025. .



Competitive salary and benefits package on offer.

Opening date: July 2nd, 2025
Closing date: July 30th, 2025 Visa mindre

At AstraZeneca, we are an equal opportunity employer that puts patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, a team leader, thinking big and working together to make the impossible a reality.

As part of the Global Human Resources team at AstraZeneca, you will have the opportunity to thrive in a fast-paced, creative and purposeful environment where bold, innovative thinking is encouraged. We believe our people are our greatest asset and are always looking for top talent whose curiosity, learning-agility and strong values orientation results in the delivery of high quality, impactful outcomes that accelerate our people and business success.

We are seeking an HR Solutions Partner for a 12-month contract to support our Operations and IT divisions. In this role, you will work closely with HR Business Partners and HR Centres of Expertise (CoE) to deliver high-quality HR support to leaders and employees. Reporting to an HR Solutions Manager who oversees a global team of HR Solutions Partners, you will be based at our Gothenburg site-a vibrant hub of innovation, home to over 2,400 colleagues from more than 50 countries. Here, diversity is celebrated as a key driver of creativity, scientific progress, and meaningful change for patients across the globe.

As an HR Solutions Partner, you will collaborate with HRBPs to provide expert guidance and coaching to managers and HR colleagues on all HR policies, processes, and programmes. You will play an important role in supporting business-specific HR initiatives in a fast-paced and evolving environment, helping to shape the future of AstraZeneca.

If you are motivated by challenge, inspired by change, and committed to making a real-world impact, we encourage you to apply and join us on our journey to push the boundaries of science and talent development.

Main Duties & Responsibilities:

* Provide generalist HR advice on a range of employment related matters (e.g., disciplinary and grievance cases, attendance management, parental leave) and escalate to Employee Relations Specialist or COEs as appropriate
* Work collaboratively with colleagues located in Global and Regional HR Center and HR Services teams in other countries to improve the customer experience, through accuracy and pace of delivery
* Deliver sound generalist HR support, acting as a key point-of-contact and a trusted partner for provision of professional advice and support to a range of HR activities and programs
* Ensure flawless execution of key people processes across the business - leading and supporting HRBP's with Performance Management, Reward, Employee Relations, change management, compensation and Workforce Planning processes
* Co-design, lead and drive key HR project delivery within the BBU, in line with defined People Plan priorities, with support, coaching and guidance from the HRBPs
* Deputise for HRBPs on key meetings and functional communication activity, where necessary
* Maintain a high level of communication with all levels of the organization (both globally and locally) and positively impact the key decisions

Essential Requirements:

* Relevant HR experience
* 0-2 years of HR experience
* Bachelor's Degree
* Practical experience providing HR advice to colleagues and senior leaders
* Excellent analytical skills
* Technical HR knowledge / skills associated one or more of the following disciplines - Resourcing, Performance & Reward, Employee Relations, L&D, organisational change
* Attention to detail; accomplishes tasks and processes accurately and completely
* Effective communicator and able to build relationships quickly
* Self-starter, being able to deliver on own initiative and prioritise independently
* Hunger for personal learning and self-driven development
* Proven project management capability
* Demonstrated ability to use Microsoft Office products is required (Word, Excel, Outlook, PowerPoint, Box)

Desirable requirements:

* Possesses knowledge and understanding of HR systems (Workday, ServiceNow)
* Experience in managing / interacting with sizeable internal customer base
* General knowledge and understanding of AZ policies and procedures

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us while we continue to build a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we are developing new ways to work, ground breaking methods, and bringing unexpected teams together. Interested? Come and join our team!

So, what's next?

Ready to make a difference? We will be reviewing applications ongoing, so apply now with your CV and cover letter, no later than 8th of July!



Explore more about:

Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Inclusion & Diversity at AstraZeneca: https://careers.astrazeneca.com/inclusion-diversity

Sustainability at AstraZeneca: https://www.astrazeneca.com/sustainability/resources.html Visa mindre

Are you a passionate individual with expertise in mathematical modelling and pharmacokinetics-pharmacodynamics (PK/PD)? Do you want to contribute to the development of future treatments for cardiovascular, renal, and metabolic diseases? If so, we invite you to join our Modelling & Simulation team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area at AstraZeneca. This position is based at our dynamic R&D site in Gothenburg, Sweden.



Accountabilities:

As a Modelling and Simulation PK/PD expert, you will play a key role in shaping project strategies and driving critical decisions across our drug discovery portfolio. You will actively influence drug project teams, guiding the selection of targets, molecules, optimal dosing strategies, patient populations, and overall development pathways.

You will have the opportunity to design and oversee the execution of complex studies in preclinical disease models, applying advanced mathematical modelling approaches to deliver impactful PK/PD and translational insights. Your expertise will enable you to synthesize data from multiple sources, predict human pharmacokinetics and pharmacodynamics, and influence the definition of efficacious exposure and dosing regimens.

In this role, you will present and defend your quantitative assessments and recommendations to internal governance and senior stakeholders, shaping critical decisions at the highest levels. You will also provide scientific leadership by initiating and leading strategic DMPK and PK/PD innovation projects, fostering collaboration across disciplines, and representing AstraZeneca's modelling expertise both internally and within the broader scientific community.



Essential Skills/Experience:

*

PhD in pharmacokinetics, pharmacology, mathematics, or related field, with a focus on model-based PK/PD approaches, preferably in a preclinical/translational setting

*

Industry or academic experience in exposure-response modelling (PK/PD, NLME, PBPK and/or QSP) including hands-on experience with scriptable modelling softwares (e.g., Phoenix, R, Matlab, Python, Monolix, NONMEM)

*

Demonstrated scientific leadership through a publication track record in relevant area

*

Excellent interpersonal skills and the ability to work in cross-functional teams

*

Excellent communication skills in English, both verbal and written



Desirable Skills/Experience:

*

Experience in pharmaceutical research and development

*

Experience in PBPK modelling (e.g. Simcyp or PK-Sim)

*

Experience in defining quantitative modelling strategies across various therapeutic modalities (e.g., small molecules, oligonucleotides, peptides, proteins, antibodies or cell/gene therapy)



At AstraZeneca, we are driven by results and use our unique blend of science and commercial knowledge to spot opportunities and drive outcomes. We are part of an expansive healthcare ecosystem that connects key players across the entire patient journey. Our patient-first approach informs every decision we make. We are committed to your development and believe that your best is better here. Join us and be part of a global team filled with the smartest minds.



Ready to make your mark? Apply now and be a part of our journey to redefine the future of healthcare! Welcome with your application no later than July 6th, 2025. Visa mindre

We are looking for an experienced Laboratory Automation Specialist (Data & Workflows) to join our team. In this key role, you will contribute to the advancement of our automated compound synthesis platform. If you are enthusiastic about enhancing laboratory workflows through automation and data-driven approaches, this is a unique opportunity to make a meaningful difference in accelerating drug discovery.

In this exciting role, you will be joining our Chemistry Automation team (iLAB) at AstraZeneca's state-of-the-art facility in Gothenburg, Sweden, where scientific excellence meets technological innovation. As part of the Compound Synthesis & Management department, we are dedicated to pushing the boundaries of drug discovery by harnessing advanced automation, data-driven solutions, and pioneering AI.

Here, you'll be immersed in an environment that thrives on collaboration and creativity, focused on accelerating the synthesis and processing of chemical compounds for biological testing. Our bold ambition is to set new industry standards, leading the way in laboratory automation and seamlessly integrating cutting-edge technologies into every step of the drug discovery journey.

In this team, your expertise will directly shape how we transform automated workflows and intelligent data handling - driving efficient, high-impact research that brings breakthrough medicines closer to patients around the world.



About the Role

As a Laboratory Automation Specialist (Data & Workflows), you will play a crucial part in developing, scripting, and managing automated laboratory workflows. Your expertise will empower our scientists to generate high-quality data more efficiently, supporting our mission to deliver life-changing medicines faster.



Key Responsibilities:

*

Collaborate with scientists, automation engineers, and IT professionals to design, implement, and optimize automated laboratory workflows.
*

Write, maintain, and troubleshoot scripts and scheduling routines for laboratory automation platforms.
*

Evaluate, integrate, and optimize laboratory scheduling and orchestration software within scientific workflows.
*

Apply data science principles to analyse laboratory data, generate insights, and enhance process efficiency.
*

Train users and provide technical support for automation software and workflow solutions.
*

Document automation protocols, workflows, and data pipelines clearly and comprehensively.
*

Stay up to date with advances in laboratory automation, data science tools, and workflow management practices.?



Essential Skills/Experience:

*

Degree in a natural science (e.g., chemistry, biology, pharmacology) or a closely related field.
*

Practical experience with data science concepts and methods.
*

Proven experience scripting for laboratory automation workflows (e.g., Python, R, C#, , or relevant automation languages).
*

Hands-on knowledge of laboratory scheduling/orchestration software (such as HighRes Cellario, Biosero Green Button Go, Automata LINQ, or equivalent).
*

Strong analytical skills with the ability to translate scientific requirements into automated solutions.
*

Excellent problem-solving and communication skills; able to work effectively within a multidisciplinary team.
*

Experience in laboratory automation or informatics is highly desirable.



What We Offer

*

Competitive salary and benefits package.
*

Opportunity to work in a multinational environment with a diverse team.
*

A culture that promotes work-life balance and employee well-being.
*

Career development opportunities across AstraZeneca.
*

The chance to contribute to the development of life-changing medicines.



Why AstraZeneca?

Join a team unlocking the power of science to treat, prevent, and potentially cure some of the world's most complex diseases. Grow your career in an inclusive environment where curiosity, collaboration, and scientific excellence are valued every day.



So, what's next?

If this sounds like your next challenge, apply today!
Applications are welcomed until June 26th, 2025.

Please note that applications must include your current CV, and a covering letter which presents your key areas of strength and why you should be considered for the role. Visa mindre

At AstraZeneca, Scientific Computing is a strategic asset underpinning our advances in science. Our research into disease and creating new medicines critically depends on continuously developing and refining best-in-class computing capabilities and the engineering teams supporting them.

We are looking for a highly motivated individual to lead HPC Infrastructure as part of our platform leadership team. If you combine excitement for HPC technology with a passion for science, and an understanding of balancing agile innovation with providing an enterprise-quality service, then we want to hear from you

The Scientific Computing platform (SCP) is AstraZeneca's primary platform supporting exploratory research, and underpins every stage of drug development from target validation through to compound selection for clinical trials. At its heart it provides some key capabilities:

*

HPC clusters on-prem, in the cloud and through external partnerships

*

Applications and software packages the scientists need to perform their research

*

Expertise to help scientists optimise their workflows and accelerate the development of new medical treatments.

A critical ability is to maintain the flexibility to adjust and adapt according to changing requirements and follow the science.

The SCP department comprises 50-60 individuals across three core technical areas (HPC Infrastructure, Software Infrastructure, and Applications), a Business Engagement team, an Operations team, and a small Program Management team.

About this role

As the HPC Infrastructure Technical Lead, you will be leading a team of 10-15 engineers and be engaged in a variety of activities including responsibility for

*

Working with scientific users to understand their needs, and develop solutions

*

Horizon scanning, identifying the future technologies needed to stay innovative

*

Defining the roadmap for the platform's HPC infrastructure

*

Prioritising the work backlog for the team according to scientific needs

*

Ensuring delivery of team objectives, both for on-premises clusters and in the cloud

*

Mentoring and coaching engineers

*

Investigating and resolving complex operational incidents

*

Ensuring the timely adoption of cloud services for all of SCP's needs



AstraZeneca is committed to promoting a healthy work-life balance, and this role is a hybrid role allowing flexible working, 60% in the office.

Essential Skills

*

Experience leading the engineering for large-scale computing environments, such as HPC, HTC for scientific research, preferably in Life Sciences (e.g. Pharmaceutical Industry, BioTech)

*

You can demonstrate a deep understanding of HPC architectures and the factors influencing their performance , including:

*

Processor and accelerator architectures

*

HPC high performance network technologies, such as Infiniband, low latency ethernet at 100Gbit and above

*

High performance storage systems (e.g. GPFS, Lustre, Weka)

*

Strong understanding of HPC scheduling systems (e.g. SLURM, LSF)

*

Strong communication skills, with the ability to explain complex technical topics to non-experts, and interpret scientific needs in terms of IT

*

Operation and configuration of public cloud computing infrastructure (e.g. AWS, Azure, GCP), especially in an HPC context

*

Experience working with distributed DevOps teams using agile methods, and using other project management techniques when appropriate

Desired Skills & Background

*

Experience optimising HPC inftastructure for applications commonly used in drug discovery; e.g. molecular dynamics, genomics and machine learning

*

Experience deploying and operating OpenStack

*

Experience with a variety of programming languages and frameworks, used in research computing and AI (MPI, C/C++, CUDA, Pytorch/Tensorflow, Python/conda, R)

*

You will have a bachelor's degree or higher in Computational, Physical or Biological Science, Engineering or equivalent area

So, what's next!

Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. If you are interested, apply now but no later than June 23.



About AstraZeneca

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for the world's most serious diseases. AstraZeneca is one of only a handful of pure-play biopharmaceutical companies to span the entire value chain of a medicine from discovery, early- and late-stage development to manufacturing and distribution, and the global commercialization of primary care, specialty care-led and specialty care medicines that transform lives.

Our primary focus is on three key areas of healthcare: Cardiovascular and Metabolic disease (CVMD); Oncology; and Respiratory, Inflammation and Autoimmunity (RIA). We are also active in the Infection, Neuroscience and Gastrointestinal (ING) disease areas. Visa mindre

HPC engineer Embark on a significant journey where your expertise in high-performance computing accelerates scientific discovery and impacts patient outcomes worldwide.

We are currently seeking a passionate, HPC engineer to join AstraZeneca's vibrant site in Gothenburg, Sweden. The ideal candidate will have extensive hands-on experience making an impact with HPC technology, delivering HPC services to a high quality, and able to relate to the scientific community and work closely with users to make the best use of research computing services.

About the Role:

At AstraZeneca, our Research Data & Analytics Team is at the cutting edge of transforming how we discover and develop medicine. As an HPC Engineer within the Scientific Computing Platform, you'll be crucial in delivering HPC services and solutions that drive progress in computational chemistry, imaging, multi-OMICs, AI and more. We're combining modern HPC with leading DevOps and cloud-native technologies to push the boundaries of biopharmaceutical research.

The HPC landscape is continually evolving. You will need the skills to help build and operate industry-leading capabilities, including application build frameworks, containerized applications and cloud software-as-a-service. Automated deployment is a key feature and you will need to be comfortable with DevOps processes and delivering consistency through automation and infrastructure-as-code.

Your Impact:

Be part of a global team where your skills in high-performance computing empower innovative scientific solutions. Engage and collaborate with researchers and engineers to optimize workflows and deploy HPC capabilities that facilitate new discoveries. Your contribution will directly enhance the development of innovative medicines, improving patient outcomes globally.

Key Responsibilities:

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Develop and operate cutting-edge research computing services and applications

*

Adopt Site Reliability Engineering principles to manage end-to-end HPC service operations, monitoring, and incident response

*

Optimize and solve complex technical problems in the HPC infrastructure and the cloud, collaborating closely with scientific users to enhance system utilization

What You Bring:

*

Proficiency in Linux environments for administration and programming

*

Solid skills in Python programming and bash scripting

*

Highly customer-focused, with the ability to communicate complex IT concepts to non-experts

*

Experience in working within a DevOps team using agile methodologies

*

Experience of building and operating services in the cloud

Desired Skills and Expertise:


*

Background in a scientific field or experience with computationally intensive scientific data analysis

*

Experience in large-scale HPC environments, parallel filesystems, and with tools such as SLURM and OpenStack

*

Familiarity with configuration automation, software distribution frameworks, and cloud deployment, especially AWS

*

Expertise in AI/ML tools, parallel programming, and containerization technologies

*

Understanding of domain-specific applications like bioinformatics tools, simulation software, or high-performance data visualisation packages

Join AstraZeneca and play a pivotal role in advancing HPC technology to accelerate scientific breakthroughs.

Apply now to be a leader in HPC innovation at AstraZeneca!



ABOUT ASTRAZENECA

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energised and rewarded for their ideas and creativity.

Where can I find out more?

AstraZeneca Gothenburg site: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. Our rich and robust pipeline provides the opportunity to work with a variety of ground-breaking medicines across diverse therapy areas and at all stages of the development process. We work to bring medicines to patients as efficiently and effectively as possible to ultimately address unmet needs across the globe. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person!

We are now looking for you who want to join us in the role as Senior Director of Central Regulatory Delivery.

This role will head the Regulatory Central Drug Delivery group, reporting to the Executive Director / Head of Regulatory Technology & Operational Excellence [RTE] group, and working alongside leaders of other pillars on the RTE leadership team. Regulatory Technology & Operational Excellence is a team of 150+ professionals working in Sweden, US, Canada, UK, Poland, Spain and India. We have a broad remit to advance regulatory capabilities at AZ through informatics, digital platforms, trusted data and reliable process.

As the Senior Director you will direct a global team that delivers operational services to Regulatory Affairs groups across all therapeutic areas. This role encompasses various accountabilities essential for the effective functioning of regulatory operations within AstraZeneca.



Typcial accountabilities:

* Lead the development and implementation of global strategies and transformations that align with AstraZeneca's regulatory mission and organizational goals.
* Oversee the central regulatory delivery team to ensure the provision of quality, cost-effective services while continuously improving technical and operational processes.
* Build and maintain effective relationships with key internal and external stakeholders to support strategic alliances and ensure compliance with regulatory requirements.
* Drive recruitment, retention, and development of a diverse and flexible workforce, balancing in-house and outsourced capabilities to meet project and business needs.
* Identify, implement, and manage innovative solutions and tools that enhance efficiency, speed, and transparency in delivery.
* Ensure all activities comply with AstraZeneca's corporate policies, GxP, external regulations, and industry best practices while fostering an information-based culture.
* Utilize data analytics to track and improve group performance globally, ensuring alignment with business objectives and KPIs.
* Represent AstraZeneca in professional forums and conferences, leveraging expert knowledge to anticipate industry trends and maintain a competitive advantage.
* Maintain awareness of AstraZeneca's product portfolio to prioritize resources effectively and ensure the availability of expertise to support medicinal product development.
* Actively contribute to the RTE Leadership Team, promoting a culture of collaboration and proactive improvements.

With this in mind we are looking for someone that strives in the role of being a strategic thinker and a visionary leader as well as being operational savvy. You are a strong communicator and a skilled relationship builder fostering a diverse workforce and nurturing team development. You have the ability to oversee the central regulatory delivery team to ensure the provision of quality, cost-effective services while continuously improving technical and operational processes.

Essential requirements

* Bachelor's degree or higher
* Minimum of 15 years of experience in the pharmaceutical industry, with significant experience in an international drug delivery role
* Proven experience directing a global team in three or more areas of regulatory operations (e.g., regulatory information, submission/dossier management, regulatory publishing, labeling/artwork, annual reports, license maintenance, or related areas)
* Comprehensive knowledge of the pharmaceutical drug development process
* Advanced understanding of regulatory guidelines and trends relating to Global Regulatory Operations (process, tools, standards)
* Experience in developing and implementing new systems and processes
* Understanding of current, as well as being visionary in, systems & technology utilized for regulatory information
* Ability to operate in both domestic and international arenas
* Capable of managing budget and productivity responsibilities
* Familiarity with GCP, GRP, and other regulatory requirements
* Proven leadership promoting motivation and empowerment of others to accomplish individual, team, and organizational objectives
* Demonstrated development of staff by identifying and providing opportunities to improve the capabilities of team members
* Strategic thinking and judgment, setting vision and expectations with customers, and applying broad business acumen into decision-making
* Demonstrated ability to manage change with a positive approach to the challenges of change for self, team, and the organization
* Excellent negotiation, collaboration, and interpersonal skills
* Strong problem and conflict resolution skills
* Demonstrated ability to set and manage priorities, resources, performance targets, and project initiatives in a global and regional environment
* Demonstrated ability to innovate best practice in Global Regulatory Operations, including experience with business process analysis and design
* Flexibility and ability to thrive in a rapid-paced environment, manage effectively, and make difficult decisions in uncertain/evolving situations
* Ability to initiate and sponsor enhancement projects within the section to build scientific and process-oriented best practices

So, what's next?
Are you ready to take the next step in your career and become part of our amazing team? We look forward to receiving your application, no later than 20 April, 2025. Visa mindre

Are you an analytical chemist with experience in automation? If so, we have an exciting opportunity for you. AstraZeneca is seeking a Senior Scientist in Automation and Analytical chemistry to join our Small Molecule Preformulation team within the Advanced Drug Delivery (ADD) function. This role is based in Gothenburg, Sweden and is part of our Pharmaceutical Sciences division.



Accountabilities:

Pharmaceutical Sciences at AstraZeneca delivers the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) and drug products. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca's therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca's clinical pipeline.

As an Analytical and Automation Senior Scientist you will drive lab efficiency and innovation by automating workflows and applying analytical expertise in the pre-clinical development phase. You will focus on various small molecule projects and develop suitable analytical techniques to risk assess formulation development for PK, PK/PD studies, and toxicology studies, but also to influence suitable choice of compounds for further development. You are expected to develop and integrate automation solutions to transform manual laboratory operations, focusing specifically on analytical tasks in the pre-clinical phase. As an analytical scientist you are anticipated to perform and evaluate assessments looking for potential degradation pathways with the use of MS data. You will develop new stability indicating methods for our pre-clinical formulations and set up methods for the validation of the quality of our pre-clinical formulations. You will also participate in scientific initiatives and technical improvement activities within the department to increase scientific knowledge and simplify our data generation and handling. You will work as a member of pharmaceutical project teams, and in close collaboration with other analysts, formulators, solid state, biopharmaceutics experts at AstraZeneca. You will independently support drug projects from the first in vivo studies to candidate drug nomination.



Key Responsibilities:

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Develop and integrate automation solutions, focusing on liquid handling and sample preparation and injection systems, such as TECAN and CTC PAL, to streamline laboratory operations.
*

Transition manual processes to automated workflows, ensuring efficiency and precision.
*

Collaborate cross-functionally to enhance lab capabilities with new technologies.
*

Conduct comprehensive analyses using advanced chromatographic techniques, with a focus on method development and stability studies and understanding.
*

Provide analytical support to drug projects from initial studies to candidate drug nomination, influencing compound selection for further development.
*

Troubleshoot and maintain automated systems, ensuring optimal performance and reliability.
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Engage in scientific initiatives to elevate knowledge and improve data handling within the department.



Essential Skills/Experience:

*

PhD or MSc with over 5 years' experience in a relevant scientific discipline (organic chemistry, analytical chemistry, pharmaceutical technology).
*

Excel in a collaborative team setting, demonstrated ability to take personal responsibility for contributions and impact.
*

Proven experience in laboratory automation, particularly using TECAN and CTC PAL systems.
*

Strong expertise in analytical chemistry techniques, including chromatography and stability assessments.
*

Basic knowledge of physical and organic chemistry for designing stable pharmaceutical formulations.
*

Proficiency in laboratory software and automation tools, with a strong understanding of GLP/GMP as well as SHE practices.
*

Ability to communicate complex scientific concepts effectively, both orally and in writing.



Desirable Skills/Experience:

*

Experience in pharmaceutical product development in the pre-clinical phase
*

Experience and knowledge in HRMS and MS/MS
*

Experience using Empower software for chromatographic evaluation.
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Innovative mindset with a drive for scientific excellence and continuous improvement.
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Excellent stakeholder management skills and the ability to simplify complex ideas.
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Industry experience in problem-solving and leading scientific projects independently. ?



To be a successful candidate for the Automation and Analytical Chemistry Specialist position, you should have experience in analytical chemistry, organic chemistry, pharmacy or similar, with focus on automation. You should be passionate about transitioning manual processes into automated workflows, focusing specifically on analytical tasks. You will also need effective communication and planning skills, balanced with the ability to work independently. An intense sense of responsibility, teamwork capability, and delivery-focused attitude are crucial for this senior scientist role.



So, what's next?

Are you ready to bring innovative ideas and fresh thinking to the table? Then you might be the person we are looking for! Please submit your application no later than 3 June 2025.

Please note that applications must include your current CV, and a covering letter which presents your key areas of strength and why you should be considered for the role. Visa mindre

Introduction to role

Are you ready to make a positive impact in a team where it means more? We are seeking a highly skilled and experienced Ontology Specialist to join our team!

Pharmaceutical Technology and Development (PT&D) is the organization that turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines and providing expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.

This is an exciting opportunity to be part of a growing capability within PT&D, focused on data. As an Associate Director Ontologist, you will be responsible for designing, implementing, and maintaining ontologies and taxonomies across PT&D. Collaborate with business and technology teams to drive improvements in the understanding and quality of our data. Join us in this role in our PT&D Governance team!

Accountabilities

The role holder will execute the following accountabilities autonomously with limited supervisory oversight:

* Design, implement, and maintain ontologies and taxonomies to support data integration across PT&D. Collaborate with data scientists, chemists, and biologists to ensure ontologies meet cross-functional needs.
* Translate complex scientific and technical concepts into structured data formats for use in data models and real-time analytics tools. Collaborate with information architects and technical teams from other departments.
* Develop and promote standards for data interoperability to facilitate seamless data exchange and integration within PT&D, across AZ business functions, and with external partners.
* Ensure high data quality and consistency by implementing quality checks and validation rules for ontology-driven systems and processes.
* Use ontology development and data curation tools to design, build, maintain and present taxonomies, controlled vocabularies, and collections.
* Understanding of enterprise data modelling tools such as IDERA E/R Studio and data catalogue tools such as Collibra.
* Deliver training and support for end-users to maximize the utilization of ontology tools and platforms.
* Stay updated with the latest trends and advancements in managing and governing controlled vocabularies, taxonomies, ontologies, and enterprise knowledge management. Encourage innovation by proposing new approaches or technologies to improve data handling.
* Evolve the ontology strategy, explain the benefits of ontologies to deliver value from data and support the development of knowledge graphs.
* Remain informed about industry-standard ontologies while thoroughly reviewing existing internal ontologies and decision frameworks to ensure alignment and informed adoption of standards.
* Adapt to rapid changes due to the introduction of automated tools and large language models (LLMs) and automation, anticipating significant evolution in responsibilities over the coming years.

Essential skills and experience

* Undergraduate degree in Computer Science, Data Management or possibly subject area (R&D, Finance, HR etc) and cross-trained or equivalent number of years of experience.
* Technology Knowledge: familiarity with industry standard ontology concepts, including RDF, OWL, SKOS, SHACL.
* Use of at least one industry standard methodology and toolset such as RDF/GitHub, Protégé, Semaphore and Neo4j.
* Proven interpersonal and communication skills to translate, promote, and embed Data Governance and Data Standards ensuring agreement across a large scale and diverse organization.
* Proven Problem-Solving skills - Proficiency in identifying issues, analysing situations, and developing effective solutions within the scope of data policy and governance.
* Experience in working in multi-skilled, multi-location data teams, working to agile principles.
* Excellent written and verbal communication, and consultancy skills.

Desirable skills and experience

* Domain data understanding: the structure, provenance, and meaning of the source data crucial to the domain.
* Enterprise Data Management: Experience of data governance, data quality, and data architecture.
* Technology Knowledge: Data technologies, including databases, data lakes, and data warehousing solutions, and tools for data visualization and reporting.
* Project Management

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

AstraZeneca offers an environment where you can be part of shaping the future of Operations. If you have the passion to accelerate growth and make a difference in people's lives, this is the place for you.

Ready to take on this exciting challenge? Apply with your CV and cover letter no later than June 5th 2025! Visa mindre

Would you like to be part of a team that is at the leading edge of bioanalysis and omics technologies? Do you aspire to work in a world-leading, innovative and cross-functional environment? Are you looking to join a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

We are seeking for a motivated and passionate individual to join us as an Associate Director, EUDiscovery Bioanalysis, Quantitative Mass Spectrometry, in our Integrated Bioanalysis (IBA) organization within Clinical Pharmacology and safety sciences (CPSS). Leading a European-based team by example, you will support ADC and biopharmaceutical drugdiscovery and development, Multi-omic studies as well as biomarker assessments for critical projects within the AstraZeneca portfolio employing mass spectrometry-based approaches. You will work at the forefront of bioanalytical sciences and play a key role in the development and progression of new medicines to the market. We are looking for an enthusiastic and innovative team player with experience of line management and detailed knowledge of Bioanalysis LC-MS workflows and demonstrated hands-on experience. You will need to use your experience and consistent track record to design, develop and deliver robust bioanalytical strategies and associated bioanalytical methods; you will need to ensure that assays are shown to be fit-for-intended purpose and provide data that will allow project teams to make informed decisions with confidence. As a Subject Matter Expert, you will be responsible for enhancing the iBA reputation for scientific excellence by presenting at internal and external meetings, and publishing manuscripts. You will be expected to represent the department on multidiscipline, cross functional, drug development teams and work alongside colleagues & stakeholders across iBA and CPSS functions and partner organisations. The position will be based at our vibrant strategic R&D site in Gothenburg, Sweden.



What you will do, your main accountabilities will be to:

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Lead a team of bioanalytical and mass spectrometry experts, based in the UK and Sweden, in non-GXP bioanalysis of large molecules
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Develop novel quantitative mass spectrometry workflows combining digestion-based or intact molecule analysis to address sophisticated bioanalytical challenges related to drug discovery and development for ADC, oligonucleotide and other drug modalities in a variety of biological matrices
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Elaborate, validate/qualify state-of-the-art mass spectrometry assays in support of pharmacokinetic, toxicokinetic, pharmacodynamic, mechanistic, safety, prognostic and diagnostic biomarkers
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Lead internal/external collaborative projects working together with safety scientist, pharmacologists, toxicologists, imaging scientists, pathologists, data scientists and translational science experts across global AstraZeneca teams
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Support effective project planning and project management, from sample arrival through to assisting with reports to collaborators
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Operate, maintain and troubleshoot a variety of recent instruments
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Serve as functional representative/expert on multidisciplinary project teams
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Adhere to established Standard Operating Procedures, industry practice and regulatory guidance as appropriate
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Contribute to validation/qualification protocols and reports, bioanalytical reports, clinical study reports, as appropriate



Requirements:

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PhD in Analytical Chemistry, Biochemistry or related field with a strong expertise in mass spectrometry for bioanalysis and antibody drug conjugates
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Innovative and influential bioanalytical leader capable of defining, leading and implementing robust bioanalytical strategies, risk mitigations and solutions to challenges in support of diverse project teams
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In depth knowledge of bioA/biomarker concepts such of "context of use or fit for purpose assay validation/qualification
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5+ years of relevant industry/biotech experience in mass spectrometry-based bioanalysis
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Experience of leading teams, with proven ability to coach, mentor and manage people to successfully deliver to projects
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Excellent skills in study design, implementation of challenging and innovative LC-MS assays and data interpretation in the field of biomolecule characterization and/or multi-omics
*

Hands-on experience in the operation of high resolution (qTOF, IMS-TOF, Orbitrap) and QqQ instruments and demonstrated experience with various acquisition modes (DDA, DIA, PRM, MRM, etc)
*

Proven track record of sample preparation and data acquisition method development and optimization and strong record of productivity and scientific publications

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Excellent organizational, documentation and technical writing skills, excellent command of English (written and oral) and strong communication and interpersonal skills



Desirable:

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Experience with a broad array of multiomics techniques including, but not limited to, proteomics, metabolomics, lipidomic, RNAseq, cell- painting or genomics applications
*

Background in bioinformatics/statistical analysis
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Familiarity with biomarker discovery and validation and with drug metabolite identification and profiling studies
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Applied knowledge of bioanalytical techniques that would strengthen the departments bioA toolbox e.g., Flow Cytometry, HPLC-MS/MS, high sensitivity immunoassay platforms, qRT-PCR, dd-PCR
*

Contributed to regulatory submission documentation such as INDs, CTAs, IBs, ISI and/or NDAs/BLAs and experience in regulatory authority responses across multiple geographies
*

Proven experience of operational streamlining and use of innovation tools, such as AI, within the workplace Visa mindre

Are you an experienced Leader for Safety Science in the early phases of Drug Discovery, and looking for your next challenge? Would you like to bring your scientific excellence and leadership skills to BioPharma Safety and become a key player in the discovery of safe innovative medicines? If yes, this might be your next career step!

AstraZeneca is looking to recruit a Senior Director for Safety Science to strengthen the Discovery Safety team and provide safety strategy guidance to our Discovery Safety Specialists/ Toxicologists supporting projects for cardiovascular, renal, metabolic, and respiratory indications. The position can be based in one of our vibrant R&D sites in Gothenburg, Cambridge, Gaithersburg or Boston.

In this role you will play an important part in the BioPharma Safety department, within the larger global Clinical Pharmacology & Safety Science (CPSS) function. As the Senior Director and Strategy Lead for the Discovery Phase, you will provide guidance on safety strategies for the discovery portfolio from target selection to candidate delivery. In this role, you will collaborate closely with the Head of BioPharma Discovery Safety and be a line manager for the Discovery Toxicologists and resources holder for the discovery phase. This role will report to the Head of BioPharma Safety and will be a member of the BioPharma Safety department leadership team.





Your main accountabilities:

As true Drug Hunting partners to BioPharma R&D, we contribute to the selection of novel drug targets, design of therapeutic concepts, identification and optimization of different modalities, and the selection of novel candidate drugs. We develop and apply cutting edge molecular, cellular and in vivo technologies to push the boundaries of predictive safety science and investigative toxicology.

*

You will be responsible for leading the safety strategies from target selection to candidate delivery with the aim to deliver molecules with the Right Safety profile.
*

Develop and apply innovative safety solutions and safety research to meet strategic needs of the discovery project portfolio of small molecules, peptides, antibodies, oligonucleotide based therapies, and to pursue cutting edge science and technologies to optimize and influence safety assessment of novel drugs.
*

Engage with world-class experts across our organization to develop, refine and implement innovative experimental strategies and use the data to assess and/or provide mechanistic understanding of safety issues (e.g. advanced in silico, in vitro and in vivo models, data and AI, advanced imaging, systems modelling)
*

Act as Discovery Safety Lead/ Toxicologist leading the nonclinical safety aspects of assigned BioPharma projects in the Discovery phase, including highly accelerated projects, and in-licensing evaluation activities.
*

Partner with Strategic Toxicology Leads, Discovery Safety leaders, Safety Innovation and Regulatory Toxicology, Safety Pharmacology, Pathology, and external partners to secure peer input.
*

Build networks with other teams, external partners and external stakeholders to learn about new developments, leverage opportunities and share best practices.
*

As a BioPharma Safety Leadership Team member, you will identify, set, and deliver on overall department objectives.





Essential Skills/Experience:

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PhD (or equivalent) in toxicology, cell biology, pharmacology, systems biology or related field, and a strong scientific track record. (other relevant job experience will also be considered).
*

Experience of project portfolio safety support in the cardiovascular, renal, metabolic, and respiratory therapy areas, as well as modalities such as small molecules, peptides, antibodies, and oligonucleotides are considered as an advantage.
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Experience with design of strategies and execution of in vitro and/or in vivo experiments to determine the safety of therapeutics.
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Preferably >5 years' experience of safety in the drug discovery phase (from project conception to candidate drug selection). Clear understanding of safety activities and strategies post candidate delivery.
*

Leadership skills and experience from handling a large and dynamic project portfolio in the pharmaceutical industry.
*

The successful candidate is a highly motivated, creative and innovative scientist and leader with a flexible, collaborative and team-oriented mindset. You like to solve problems in a goal-focused fashion, and you have strong communication and presentation skills. Along with this, you have a social personality and will enjoy contributing to our open, positive, collaborative working climate.





So, what's next!

If you want to be a part of pushing the boundaries of science with us - apply today!

Please submit your application no later than 21st May 2025. Visa mindre

At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's outstanding skills with those of people from all over the globe!

AstraZeneca's vision is to help patients by redefining the treatment paradigm, with a broad pipeline of next-generation medicines. We're investing to enhance our understanding of disease as we work towards creating the next generation of therapeutics and pioneering new approaches to better predict clinical outcomes. We harness digital, data science & AI to fast-forward our research. Making sure work born in a lab can make a real difference. Working here means that every day you will be impacting patients' lives across the world.

AstraZeneca, Global Patient Safety (GPS) is at the forefront of defining and optimizing the safety profile of our medicines across their lifecycle in all therapeutic areas. GPS leads the way in integrating science, data, and technology to shape clinical safety strategies. From monitoring and detection to characterization and reporting of adverse events, GPS plays a critical role in ensuring the safety of our medicines for patients worldwide.

As a Medical Director, Senior Patient Safety Physician in Patient Safety BioPharma, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. BioPharma Global R&D drives our innovative pipeline, redefining science into valued new medicines and ensuring patients around the world can access them.

Main Duties and Responsibilities:

In this role, you'll be responsible for the Clinical Safety strategy for assigned drug projects and products throughout all stages of development and/or when on the market, including implementation and communication of the strategy at the project team/governance level. Essentially, the continued safety assessment, evaluation and risk management of AZ products or product groups in various stages of clinical development and/or the post-marketing setting as well as the continuous efficient evaluation of adverse event and all other safety information will be within the remit and scope of this role.

You will provide consistent communication of safety topics across all regulatory safety documents, e.g. Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experience Reports (PADERs) and Development Safety Update Reports (DSURs), for assigned product(s)/program(s).

You will proactively evaluate the clinical implications of safety data from pre-clinical studies, clinical studies, literature to predict / establish the safety profile of compounds in clinical development. This process includes employing expert groups and methodologies such as Safety Knowledge Groups (SKG's), Safety Science, Informatics expertise, modeling and simulation to manage the risk to patients. Additionally, you'll be involved in all safety surveillance activities, that may include medical review of individual safety cases (providing medical expertise and judgment), signal detection, evaluation and safety information review committee activities for all products in area of responsibility.

This role will also require your medical input and review of periodic reports (e.g. PBRERs, PSURs, or DSURs) and renewal documentation submitted to regulatory agencies and the patient safety contribution to global regulatory submissions (NDA, BLA, MAA etc.) for new products, formulations or indications.

Essential Education, Experience and Skill Requirements

* Medical degree (e.g. MD, MBBS).
* High level of medical competence, with an ability to balance this with industry standards to achieve business goals.
* Scientific track-record in a specialty relevant to PSTA Biopharma.
* At least 3+ years of clinical experience in a specialty relevant to PSTA Biopharma.
* Ability to work effectively in an advanced matrix structure.
* Proficient in written and verbal English.



Preferred Education, Experience and Skills

* PhD in scientific field relevant to PSTA Biopharma.
* Experience managing and coaching peers (e.g as a line manager and/or leading a research team).
* Documented experience as Principal Investigator in clinical trials or at least 2+ years of Drug Development/Patient Safety experience with clear evidence of delivery.
* Scientific expertise in cardiovascular medicine or a closely related field.



Location: Onsite 3 days/week in Gothenburg, Sweden

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.

So what's next?
Are you already envisioning yourself joining our team? Good, because we can't wait to hear from you! We will be reviewing applications and shortlisting on a rolling basis - as such we reserve the right to withdraw this vacancy ahead of the stated closing date Visa mindre

Are you passionate about applying computational approaches to solve problems in biomedicine? We are now looking for an Industrial PhD student in Data-Driven Life Sciences to work on a cutting-edge project in collaboration with AstraZeneca Chalmers University of Technology, funded through the Wallenberg National Program for Data-Driven Life Science (DDLS).

The future of life science is data-driven. Will you be part of that change? Then join us in this unique Program!



The research group: The PhD student will be based both at AstraZeneca, Gothenburg, and at Chalmers University of Technology. At Chalmers, the student will be a part of the Holme Lab, based at the Division of Chemical Biology, Department of Life Sciences (LIFE). The Holme Lab is a multidisciplinary team of researchers addressing questions and challenges related to lipid self assembly in systems such as lipid nanoparticles (LNPs), extracellular vesicles and cell membrane mimics. We use a variety of single particle techniques as well as small angle scattering experiments to identify lipid self-assembly on a structural level, and correlate this with in vitro functional activity.

At AstraZeneca, the student will be integrated into the Data Science and Modelling department within the Pharmaceutical Sciences division. This multidisciplinary team utilises a combination of machine learning and mechanistic modelling to derive models and scientific insights from data, which both support and enhance drug development projects, and drive science forward.

This position is one of several industrial PhD roles funded by the DDLS program, which supports training in four strategic areas: cell and molecular biology, evolution and biodiversity, precision medicine and diagnostics, and epidemiology and biology of infection. At Chalmers University of Technology and AstraZeneca we are announcing the position as DDLS PhD student in data-driven precision medicine and diagnostics. This covers data integration, analysis, visualisation, and data interpretation.



The project:

The industrial PhD student will develop a comprehensive framework that integrates multiscale molecular dynamics (MD), AI and machine learning (ML) approaches, that together with biophysical characterisation techniques will advance the current state of lipid nanoparticle (LNP) understanding and its design. This research will focus specifically on enhancing targeted delivery systems for immunotherapy applications, representing a cutting-edge frontier in drug delivery science.

The student will work closely with Dr. Martina Pannuzzo (Associate Principal Scientist), Dr. Felix Faber (Associate Principal Scientist) and Dr. Suzy Jones (Associate Principal Scientist) at AstraZeneca, and Dr. Margaret Holme (Assistant Professor) at Chalmers, within a cross-functional and dynamic research environment. This is a unique opportunity to shape the future of data-driven drug delivery at the intersection of computational biophysics, AI/ML modelling, and biophysics/chemistry-driven approaches to understanding and developing therapeutic lipid nanoparticles.



Focus areas of the position:

*

Chemistry, biophysics
*

Machine learning and generative AI
*

Molecular modeling and molecular dynamics simulations
*

LNP formulation and characterisation including e.g. small angle scattering, microscopy, single particle analysis techniques



Essential skills/experience

*

We welcome applications from highly motivated candidates with a Master of Science degree (or equivalent, 240 ECTS) in Computer Science, Chemistry, Life Sciences, or a related field.
*

Strong programming skills in Python
*

Good understanding of chemistry and biology concepts
*

Excellent communication skills in English (oral and written)



Desirable skills/experience

*

Experience in deep learning/generative AI or molecular modelling
*

Prior research or industrial exposure
*

Ability to work in a multidisciplinary and collaborative environment



How to apply: The application, written in English, is submitted through the application portal of AstraZeneca and should include:

*

Cover letter stating your motivation and relevant qualifications
*

CV including academic achievements, technical skills, and at least two references
*

Copies of certificates, degrees, grades, and (if applicable) TOEFL test results

Start date: 2025-09-01 or otherwise agreed. Type of employment: Temporary position, 4 years

If you're excited by the possibility of joining a program that merges AI and pharmaceutical innovation, apply no later than May 13, 2025. We look forward to your application! Visa mindre

At AstraZeneca, we transform innovative ideas into life-changing medicines. By joining us, you're embarking on a journey where big thinking and collaboration turn the impossible into reality. We are committed to revolutionizing medicine and embracing scientific breakthroughs to address the unmet needs of patients across the globe. We dedicate our efforts to areas where we can make significant impacts and breathe life into groundbreaking ideas.

The Opportunity

Join us as Director, Cloud Advisory at our vibrant R&D site in Gothenburg Sweden. In this role you will be part of the global Cloud Enablement team, which plays a crucial role in unlocking the potential of our multi-cloud environments. This opportunity is perfect for someone passionate about delivering high value cloud-based solutions across an expansive enterprise and enjoys working in a fast moving and dynamic environment.

Role Overview

We are seeking a visionary leader to join a global team focused on enabling the R&D business in AWS, Azure, and Google Cloud technologies. In this pivotal role, you will engage senior stakeholders in order to understand their strategic objectives and how cloud technologies can accelerate their delivery. Working with our team of cloud solution engineers, you will be a catalyst in advising project, product, and platform teams, driving value through strategic cloud adoption and optimization strategies.

The role holder is accountable for the cloud estate underpinning R&D's platforms and applications, specifically for defining the demand plan, required resources and ensuring successful delivery of cloud solutions. A focus on innovation, automation and continuous improvement is required to improve efficiency and effectiveness.

Key Responsibilities

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Demand & Delivery Management: Engage executives to accelerate business outcomes through cloud solutions. Capture and forecast the demand for cloud services to ensure the successful deployment of projects.

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Continuous improvement: Establish and own mechanisms that improve cycle times and reduce waste. Promote Lean/Agile ways of working and mind-sets.

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Customer Experience: Ensure feedback mechanisms are in place to understand and respond to customer sentiment

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Stakeholder Management: Identify and manage key stakeholders, ensuring they understand the opportunities and challenges around cloud adoption

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Vendor Management: Build strong relationships with cloud service providers to negotiate contracts and explore new services or technologies.

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Innovative Leadership: Stay at the forefront of emerging cloud technologies, advising on industry trends and potential opportunities.

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Cloud Strategy Development: Collaborate with stakeholders to craft and implement a cloud strategy that aligns with business goals and cutting-edge technological advances.

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Performance Optimization: Continually improve cloud performance through optimization, cost-saving initiatives, and capabilities enhancement.

Qualifications & Skills

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Bachelor's degree in Computer Science, Information Technology, or related field.

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Proven experience of project or solution delivery in cloud environments. Ability to manage multiple projects and priorities in a dynamic environment.

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Good understanding of cloud platforms (e.g., AWS, Azure, Google Cloud) and associated services.

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Superior communication skills to convey technical ideas effectively to non-technical audiences.

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Experience of working in agile teams using methodologies such as SCRUM and SAFe and use of Jira and Confluence

Preferred Skills

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Cloud certifications

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LEAN/Agile certifications

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Experience in managing hybrid and multi-cloud strategies.



Apply Today

Be part of a visionary company that values diversity, inclusion, and innovation. If you're ready to embrace this exciting leadership role and drive AstraZeneca's success, we want to hear from you!

We welcome your application today but no later than May 7 at the latest. Visa mindre

Do you have expertise and experience in PK, PKPD, mathematical/statistical modeling and simulation, and Model Informed Drug Development (MIDD) and its application in drug development? Would you like to apply your knowledge in a company that is dedicated to following the science and turning ideas into life-changing medicines? If so, this could be your next challenge!

We have an exciting opportunity for an engaged and diligent individual to join our Clinical Pharmacology and Quantitative Pharmacology (CPQP) team at AstraZeneca at our vibrant site in Gothenburg, Sweden, in the role as a Clinical Pharmacometrician at an Associate Director or Senior Scientist level (depending on your background, experience and skills). This is a global position that will support large- and small molecule projects across all phases of clinical development within the therapy area of Cardiovascular, Renal and Metabolism.

Within the Clinical Pharmacology and Safety Sciences (CPSS) function at AstraZeneca, we have a groundbreaking Clinical Pharmacology and Quantitative Pharmacology (CPQP) organization with a diverse and uniquely skilled team of Clinical Pharmacometricians and Clinical Pharmacology Leads. You will thrive in an environment that inspires innovation, encourages multidisciplinary team-working and collaboration with academia, and rewards original scientific thinking.


What you will do
Working closely with clinical pharmacologists, physicians, statisticians and other scientists, you will apply model informed drug development (MIDD) to contribute to clinical programs, to support the design and interpretation of clinical studies and influence key decisions in early and late clinical development.

The work includes integration of relevant data, such as dose information, pharmacokinetics, biomarkers and clinical endpoints within and across studies, compounds and development stages. Use of simulations and pharmacometric/statistical analyses to inform trial and program designs and decisions are important focus areas for us.

In collaboration with clinical pharmacologists, you will represent CPQP in cross-functional clinical project teams and be responsible for identifying and driving model informed drug development opportunities, to accelerate and advise decision making. Based on your interest, skills and experience, you might also take on strategic planning and delivery of the clinical pharmacology strategy acting as a dual Clinical Pharmacometrician/Clinical Pharmacologist. You will communicate your findings within and outside of AstraZeneca and publish in peer reviewed journals.



Minimum requirements for the role

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PhD in pharmacometrics or mathematical/statistical modeling and simulation or other relevant area
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Strong quantitative skills (e.g. experience in population modelling, statistics, systems and translational pharmacology modelling)
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Strong technical knowledge and hands-on skills in PK and PK/PD modeling and simulation including training and experience with pharmacometric and statistical software (NONMEM, R, Stan, Monolix, Phoenix)
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Knowledge in pharmacology and drug targets
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Excellent oral and written communication skills



Desirable requirements

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3+ years of industry experience or equivalent in quantitative modelling and its application in drug development
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Track record in creating and delivering on MIDD strategies in clinical drug development programs for both small and large molecules
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Early and late phase clinical development experience
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Understanding of clinical pharmacology aspects of drug development, preferably in both a small and large molecule setting
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Recognized scientific expertise demonstrated by scientific publishing in the field of clinical pharmacometrics/pharmacology
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Knowledge in Cardiovascular, Renal or Metabolism disease areas



Why AstraZeneca?

At AstraZeneca, we are at the forefront of medical innovation. We use our unique position as medical leaders across our enterprise and the healthcare ecosystem to shape the future of healthcare. We provide medical leadership across the whole product lifecycle - from advising on Research & Development investment decisions, to leading pre-launch scientific efforts and accelerating evidence-based healthcare changes in the real world. We are networkers and influencers by nature. In our role as scientific ambassadors, we thrive on working with people internally and externally.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



So, what's next?

Are you prepared to bring your innovative ideas and fresh perspectives to the table? If so, you might be the candidate we're seeking! Please submit your application by 11th May 2025.

Please ensure your application includes your current CV and a cover letter highlighting your key strengths and explaining why you should be considered for the role. Visa mindre

Embark on a significant journey where your expertise in high-performance computing accelerates scientific discovery and impacts patient outcomes worldwide.

We are currently seeking a passionate, HPC engineer to join AstraZeneca´s vibrant site in Gothenburg, Sweden. The ideal candidate will have extensive hands-on experience making an impact with HPC technology, delivering HPC services to a high quality, and able to relate to the scientific community and work closely with users to make the best use of research computing services.

About the Role:

At AstraZeneca, our Research Data & Analytics Team is at the cutting edge of transforming how we discover and develop medicine. As an HPC Engineer within the Scientific Computing Platform, you'll be crucial in delivering HPC services and solutions that drive progress in computational chemistry, imaging, multi-OMICs, AI and more. We're combining modern HPC with leading DevOps and cloud-native technologies to push the boundaries of biopharmaceutical research.

The HPC landscape is continually evolving. You will need the skills to help build and operate industry-leading capabilities, including application build frameworks, containerized applications and cloud software-as-a-service. Automated deployment is a key feature and you will need to be comfortable with DevOps processes and delivering consistency through automation and infrastructure-as-code.

Your Impact:

Be part of a global team where your skills in high-performance computing empower innovative scientific solutions. Engage and collaborate with researchers and engineers to optimize workflows and deploy HPC capabilities that facilitate new discoveries. Your contribution will directly enhance the development of innovative medicines, improving patient outcomes globally.

Key Responsibilities:

* Develop and operate cutting-edge research computing services and applications
* Adopt Site Reliability Engineering principles to manage end-to-end HPC service operations, monitoring, and incident response
* Optimize and solve complex technical problems in the HPC infrastructure, collaborating closely with scientific users to enhance system utilization

What You Bring:

* Proficiency in Linux environments for administration and programming
* Solid skills in Python programming and bash scripting
* Highly customer-focused, with the ability to communicate complex IT concepts to non-experts
* Experience in working within a DevOps team using agile methodologies

Desired Skills and Expertise:

* Background in a scientific field or experience with computationally intensive scientific data analysis
* Experience in large-scale HPC environments, parallel filesystems, and with tools such as SLURM and OpenStack
* Familiarity with configuration automation, software distribution frameworks, and cloud deployment, especially AWS
* Expertise in AI/ML tools, parallel programming, and containerization technologies
* Understanding of domain-specific applications like bioinformatics tools, simulation software, or high-performance data visualisation packages



Join AstraZeneca and play a pivotal role in advancing HPC technology to accelerate scientific breakthroughs.

Apply now but no later than 21st of April to be a leader in HPC innovation at AstraZeneca!

ABOUT ASTRAZENECA

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energised and rewarded for their ideas and creativity.

Where can I find out more?

AstraZeneca Gothenburg site: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre

Are you an experienced drug discovery scientist with expertise in pharmacokinetics, pharmacology and drug metabolism (DMPK)? Would you like to apply your expertise in a global company that follows the science and turn ideas into life changing medicines? Then you could be the new colleague we are looking for!



We are now looking for an experienced and motivated individual to join the team as a DMPK Project Leader. The position is placed at AstraZeneca's dynamic R&D site in Gothenburg, Sweden. Working at AstraZeneca means being entrepreneurial, following the science, scrutinizing data and details simultaneously with holistic thinking and through teamwork make progress. Your level of professional experience will be relevant for your initial career level (Associate Principal Scientist or Principal Scientist).



Respiratory & Immunology (R&I) is one of the three main therapeutic research areas within AstraZeneca. Early R&I is a global function, with research units in Gaithersburg (US), Cambridge (UK) and Gothenburg (Sweden), and delivers candidate drugs into late-stage clinical development. DMPK interacts with other functions in supporting Early R&I projects all along the value chain, from target selection all the way to market launch and Life cycle management.



What you'll do:
With a true passion for drug discovery you will support our portfolio within the R&I therapeutic area. In the DMPK project lead role you will work collaboratively with project representatives from other disciplines. These may include biology, antibody Discovery/Protein Engineering, medicinal chemistry, safety, clinical pharmacology, and pharmaceutical sciences, where your task is to influence candidate profiling by providing the necessary DMPK support for clinical investigations.



It is your responsibility to ensure delivery of all DMPK related activities. These include preclinical PK experiments, in vitro ADME and biotransformation to yield pharmacokinetic understanding. Furthermore, assisting design of pharmacodynamic studies that ultimately delivers a pharmacological assessment underpinning human dose prediction.



You will work on projects from candidate selection to Phase 2a. We believe that you have a solid understanding of DMPK, a working knowledge of pharmacology, and that you will be able to provide expert advice and interpretation of complex drug discovery data.



Main Duties and Responsibilities
* Communicate scientific progresses both externally and internally
* Deliver DMPK input and data to projects within agreed timelines and to the right quality
* Apply an understanding of DMPK to support/influence compound profiling, project progression and project strategy
* Define and deliver a translational quantitative PKPD strategy in projects, so that effective conclusions can be made
* Contribute to estimation of safety margins and report results and interpretations to project teams and internal governance bodies
* Responsible for leading, coordinating and engaging with R&I DMPK colleagues in project related activities
* Prepare clear presentations related to the above for internal governance bodies

Essential requirements:
* PhD or equivalent experience in a relevant field
* Expert in DMPK sciences with profound knowledge of drug discovery and development processes
* Broad experience across different modalities (small molecules & biologics) drug development (PK & Bioanalysis)
* Experience with regulatory submissions for biologics and small molecules
* Good knowledge of all DMPK assays including the use of in silico tools for PK prediction
* Experience in project leadership
* Collaborative mindset
* Team player
* Proactive and good communication skills

Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Work policy:
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

What's next!
If you are ready to make a difference - apply today, and we'll make it happen together! We welcome your application until April 30, 2025.

Where can I find out more?

Life at AstraZeneca

This is what we're made of

Relocate to Gothenburg Visa mindre

Do you have extensive Drug Metabolism and Pharmacokinetic (DMPK) expertise with a background in medicinal chemistry, pharmacy, pharmaceutical science and/or drug discovery, and would you like to apply your expertise in a global company that follows the science and turns ideas into life-changing medicines? Then you could be the new colleague we are looking for!

We are now seeking an experienced and motivated individual to join the team as a Preclinical DMPK Project Leader (Senior Scientist/Associate Principal Scientist/Principal Scientist, depending on your level of professional experience), preferably with experience across multiple modalities.


At AstraZeneca Respiratory & Immunology, we're proud to have an outstanding workplace culture that encourages innovation and teamwork. We are united by our vision to push the boundaries of DMPK science to transform ideas into medicines for R&I patients. Employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

What you'll do:
In the role you would work collaboratively with discovery project representatives from other disciplines including medicinal chemistry, biology, safety and pharmaceutical sciences. You will influence drug design and optimization of ADMET (absorption, distribution, metabolism, excretion, toxicity) properties. Hence, it is your responsibility to ensure delivery of all DMPK related activities, including in vitro ADME, biotransformation, bioanalysis, preclinical PK and PD underpinning human dose prediction to early drug projects from target selection to candidate drug selection. We believe that you have a solid understanding of DMPK and chemistry and that you will be able to provide expert advice and interpretation of complex drug discovery data.

Main Duties and Responsibilities
* Responsible for leading all DMPK related activities, including coordinating and engaging with internal and external DMPK colleagues and collaborators, on project related activities. Deliver DMPK input and data to projects within agreed timelines and to the right quality to ensure that DMPK challenges are thoroughly assessed and resolved.
* Contribute to the design of preclinical in vivo studies to answer crucial project questions.
* Accountable, together with other functions such as Medicinal Chemistry, Bioscience and Safety, for compound design and effective cross-discipline optimization. Apply an understanding of DMPK and PKPD to support/influence project progression and strategy as well as providing the framework for human dose predictions.
* Prepare clear presentations related to the above for internal governance interactions

Essential requirements:
* PhD in Medicinal, Organic or Physical Chemistry or bio-pharmaceutics/pharmacokinetics or equivalent experience in a relevant field
* Formal training or proven experience of working with pharmacokinetics and drug metabolism and a good understanding of pharmacodynamics
* Understanding of correlations between physicochemical characteristics and their influence on DMPK properties and subsequent design of new compounds
* Have (at least) basic PK modelling skills, experience of human dose and PK prediction as well as understanding of disease biology and linking to PKPD understanding
* Extensive experience (5+ years) of working in preclinical DMPK
* Experience from drug discovery, cross-functional working and compound/project progression
* Ability to engage and collaborate across boundaries with a problem solving attitude and focus on delivery
* Strong communication skills



Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development



What's next?
This is an exciting opportunity for a talented DMPK scientist to join a strong, dynamic team and support the portfolio of a major pharmaceutical company that has science at its heart whilst being based in the beautiful city of Gothenburg, Sweden. If you are ready to make a difference - apply today and together we will make it happen! We welcome your application until April 30, 2025.


Find Out More:

Life at AstraZeneca

This is what we're made of

Relocate to Gothenburg Visa mindre

Join our BioPharmaceuticals Medical team, where we strive to provide healthcare decision-makers around the world with the evidence and confidence they need on AstraZeneca therapies. We are looking for an Evidence Delivery Associate Director to lead or support the operational planning, delivery, oversight, and budget management of company sponsored research. This is a great opportunity to shape the future of healthcare and be part of changing the practice of medicine forever!

As Evidence Delivery Associate Director, you will be based in our strategic R&D site in Gothenburg. Sweden and be a vital part of our BioPharmaceuticals Medical (BPM) Global Evidence Portfolio Delivery organization. BPM is accountable for the operational delivery of global strategic studies required to generate the evidence to build the confidence on AstraZeneca therapies required by Global Product Teams and Global Medical Teams. We aim to lead AstraZeneca in achieving scientific leadership, being a great place to work, and keeping patients at the core of everything we do.



What you will do

You will lead or support the operational planning, delivery, oversight and budget management of company sponsored research. The majority of the evidence delivered is conducted by one of our preferred CRO partners. The studies may be interventional or observational, including both primary data collection or secondary data collection. You may also help to coordinate the efforts of extended team members, notably the scientific study leader (epidemiologist for observational studies, Medical Affairs Leader for interventional studies). As Evidence Delivery Associate Director, you may own specific areas or deliverables within a study, or in some cases, assume the accountabilities of a team leader for study delivery. One important task will be leading delivery through oversight of our preferred CRO or a third-party vendor. In addition, you will support BPM Evidence's continuous improvement by developing expertise in a specific area of study delivery, serving as a point of contact for best practice, and contributing to the development and maintenance of guidance documents and training materials.

As Evidence Delivery Associate Director your focus will be to lead and project manage Company Sponsored Observational and Interventional Research studies. Independent of the study type, key accountabilities of the Evidence Delivery Associate Director will be:

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Management of study Governance processes
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Management of internal and external stakeholders
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Project Management of accountable study areas and oversight of CRO/Vendors to deliver according to cost, time and quality
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Finance Management support
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Support of study Risk Management and Quality Management activities
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Study compliance



Essential Skills/Experience

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Bachelor's degree required preferably in medical or biological science or equivalent by experience
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Extensive pharmaceutical industry/CRO experience within clinical study/research project delivery, GCP/ICH, drug development process and relevant guidelines for a specific therapeutic and geographical area (EU, US and ROW)
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Excellent influencing and proven extensive project management skills including scope, budget, timeline and team management.
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Scientific awareness and extensive knowledge of observational study guidelines and SOPs
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Extensive knowledge of early and late-stage Pharmaceutical Development
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Proven capability to collaborate effectively and successfully engage with Clinical Research Organizations and external partners
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Proven skill in building networks, collaborating successfully with diverse teams across different regions, functions, and cultural backgrounds externally and within the organization
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Persuasive communicator in English with a proven ability to work collaboratively in a multi-cultural environment
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Open to periods of travel





Why AstraZeneca?

At AstraZeneca, we are at the forefront of medical innovation. We use our unique position as medical leaders across our enterprise and the healthcare ecosystem to shape the future of healthcare. We provide medical leadership across the whole product lifecycle - from advising on Research & Development investment decisions, to leading pre-launch scientific efforts and accelerating evidence-based healthcare changes in the real world. We are networkers and influencers by nature. In our role as scientific ambassadors, we thrive on working with people internally and externally.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



So, what's next?

Are you ready to bring innovative ideas and fresh thinking to the table? Then you might be the person we are looking for! Please submit your application no later than 24 April 2025. Visa mindre

Are you ready to power the business to have a bigger impact on patients' lives?

Embrace the novel opportunity to work at a business that puts patients first. In Early Science, we have highly skilled scientists in our labs who experiment and support complex drug projects. The environment is driven by scientific and technical innovation with a high level of diversity in workflows, data, and vendors. The Digital Lab platform works to create an IT environment that digitizes the experimental process across R&D labs globally and makes experiment data more available and re-usable.

About the role:

We are seeking a detail-oriented Release Manager to join our team in Gothenburg, Sweden. You will initially be focused on establishing good release management process for our new SaaS-based Electronic Laboratory Notebook (ELN) product. This role is pivotal in managing the coordination and communication of configuration changes within our software applications. The ideal candidate will have a strong background in project management and stakeholder engagement, with the ability to ensure smooth releases in a dynamic environment.

Scope and Deliverables:

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Release Coordination: Oversee the planning, scheduling, and execution of software releases (including both internally developed components and SaaS components), ensuring that all activities are synchronized across delivery teams and stakeholders.

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Communication Management: Serve as the primary liaison between development, operations, business teams, and external partners. Facilitate clear and effective communication to ensure that all parties are informed of release activities, changes, and impact.

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Change Management: Collaborate with teams to understand configuration changes and their implications. Ensure all changes are documented, reviewed, and approved before implementation.

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Stakeholder Engagement: Work closely with business stakeholders to align release schedules with strategic goals and objectives. Gather and incorporate feedback to continually improve the release process.

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Process Improvement: Identify and implement best practices and process improvements to streamline release management activities, enhancing efficiency and minimizing risk.

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Risk Management: Assess and manage risks associated with release activities. Develop contingency plans to address potential issues without disrupting operations.

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Performance Tracking: Monitor and report on release performance metrics. Use insights to drive process enhancements and increase effectiveness.

What we are looking for:

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Release management is your passion and your career. While a SaaS platform may not have the level of automation required by bespoke software, it still has the constant change from multiple directions that keep you learning and the complexity of internally built integrations.

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You understand that details matter. IT teams need to be coordinated, change management needs to be done, rollback plans need to be in place. Business teams need to know what they will see different, when they will see their requests implemented, and need to have confidence that it will be right the first time.

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You are a constant communicator. Communication is the foundation for a solid release process.

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You'd rather fix a problem than point a finger. Vendor, configuration people, integration teams, and stakeholders might need to be pulled together into a single conversation that can just makes things work.

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Growth is important to you. You have the capacity to extend yourself from the ELN product and support good practice in the entire Digital Lab platform.



Are you ready to rise to the challenge of shaping the future of an evolving business in the technology space?

Apply now but not later than April 22nd and join us in our mission to improve lives across the world!

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Why AstraZeneca?

AstraZeneca is a place where innovation meets large-scale impact. We are dedicated to combining science with our knowledge, to deliver greater value for patients every day. We take data seriously, turning complex information into life-changing and practical insights. Here we are putting data at the heart of our processes at AstraZeneca. We work on everything from building data solutions, modelling and structuring, to exploring and innovating with data. Lead the way as AstraZeneca works towards becoming a digital and data-led enterprise. Visa mindre

Do you have expertise in, and passion for AI? Would you like to apply your AI modelling expertise in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the place for you!

As an AI Engineer, you will contribute to the development and implementation of AI solutions across a variety of domains. Your work will involve designing and building AI systems that process and analyse diverse types of data, from structured datasets, to text, multimedia content. You'll engage in enhancing machine learning pipelines and explore different AI technologies and methodologies whilst deployed as a team member on portfolio use cases within Enterprise AI Services.

Accountabilities:

Machine Learning

* Assist in designing and implementing machine learning models for various applications.
* Support tasks involved in building and maintaining machine learning pipelines.
* Help improve model performance using techniques such as optimisation and efficiency enhancements.
* Participate in data and model validation and ensure high data quality standards.

Software Engineering

* Contribute to the development of reusable software components and APIs for AI solutions.
* Assist in constructing scalable systems for data management and processing.
* Participate in writing clean, maintainable, and well-documented code to support AI projects.

Cloud & Infrastructure

* Learn and assist in setting up cloud-based architectures for AI model deployment.
* Support the development of automated processes for the continuous integration and deployment of AI models.
* Contribute to optimising AI systems for performance, cost, and scalability.
* Assist in containerisation using tools like Docker and Kubernetes and help set up monitoring for deployed systems.

Specialist Areas

* Explore different AI technologies, such as computer vision, natural language processing, and predictive analytics.
* Engage in learning activities and projects that enhance your understanding of specialised AI applications.
* Support the integration of AI technologies into broader business solutions.



Required Skills

Machine Learning

* Strong expertise in either optimisation, predictive modelling, computer vision or natural language processing
* Experience with ML frameworks (PyTorch, TensorFlow)
* Understanding of transformer architectures and attention mechanisms
* Knowledge of model optimisation and compression techniques

Software Engineering

* Degree in Computer Science, ML, or related field
* Proficiency in Python and software engineering best practices
* Strong understanding of data structures and algorithms
* Knowledge of API design and development

Cloud & Infrastructure

* Experience with major cloud platforms (AWS, Azure, GCP)
* Understanding of containerisation and orchestration (Docker, Kubernetes)
* Knowledge of MLOps tools and practices
* Experience with CI/CD pipelines and automation
* Understanding of scalability and reliability patterns

Desirable Qualifications

Machine Learning

* Experience with foundation models (CLIP, Stable Diffusion, SAM)
* Knowledge of ML monitoring and observability
* Experience with real-time inference optimisation

Software Engineering

* Contributions to open-source ML projects or libraries
* Knowledge of software design patterns

Cloud & Infrastructure

* Experience with ML deployment platforms (KubeFlow, MLflow)
* Knowledge of serverless architecture patterns
* Experience with infrastructure-as-code (Terraform, CloudFormation)



Why AstraZeneca?

At AstraZeneca, we follow the science to explore and innovate. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. We are committed to making a difference by fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. We are driven by our shared belief in What Science Can Do. A belief in its potential to redefine what's possible. We are always listening and learning from people who live with the diseases our medicines treat. It enables us to better understand their needs and, ultimately, diagnose and design the right treatments to impact patients' lives.

What's next?

If you're ready to embark on this exciting journey, please submit your application by April 27th at the latest. Applications will be screened on a continues basis.

Additional information

Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Life in Gothenburg: https://www.movetogothenburg.com/
Make a move to Global Gothenburg: https://www.youtube.com/watch?v=c-Iqbb4aw38 Visa mindre

Are you passionate about applying computational approaches to solve problems within chemistry and biology? We are now looking for an Industrial PhD student in Data-Driven Life Sciences to work on a computational drug metabolism project in collaboration with AstraZeneca and Chalmers University of Technology, funded through the Wallenberg National Program for Data-Driven Life Science (DDLS).

Chalmers University of Technology conducts research and offers education in technology, science, architecture, and maritime engineering. Chalmers is known for its multidisciplinary collaborations and strong innovation culture. The Department of Computer Science and Engineering (CSE) is a joint department between Chalmers and the University of Gothenburg. The AI Laboratory for Molecular Engineering (AIME), led by Dr. Rocío Mercado Oropeza, applies machine learning to molecular engineering problems in life sciences and drug discovery, and is based in the Division for Data Science and AI within the CSE Department.

AstraZeneca is a global, science-led biopharmaceutical company (www.astrazeneca.com). At our Gothenburg R&D site, we bring together over 2,400 employees from more than 70 countries to deliver innovative medicines. The Medicinal Chemistry and DMPK departments within AstraZeneca's Early Cardiovascular, Renal and Metabolism (eCVRM) therapeutic area are leading efforts in the design of new chemical entities and understanding their pharmacokinetic properties including how the compounds are metabolized to ensure safe and effective drug development.

Data-driven life science (DDLS) uses data, computational methods and artificial intelligence to study biological systems and processes at all levels, from molecular structures and cellular processes to human health and global ecosystems. The SciLifeLab and Wallenberg National Program for Data- Driven Life Science (DDLS) aims to recruit and train the next generation of data-driven life scientists and to create globally leading computational and data science capabilities in Sweden. The program is funded with a total of 3.7 billion SEK (about 290 MUSD) over 12 years from the Knut and Alice Wallenberg (KAW) Foundation. In 2025 the DDLS Research School will be expanded with the recruitment of 19 academic and 7 industrial PhD students. During the course of the DDLS program more than 260 PhD students and 200 postdocs will be part of the Research School. The DDLS program has four strategic research areas: cell and molecular biology, evolution and biodiversity, precision medicine and diagnostics, epidemiology and biology of infection. For more information, please see https://www.scilifelab.se/data-driven/ddls-research-school/

The future of life science is data-driven. Will you be part of that change? Then join us in this unique Program!

The research group: The PhD student will be based primarily at AstraZeneca, Gothenburg, with the possibility to spend part of their time at Chalmers University of Technology. At Chalmers, the student will be a part of the AIME research group, which focuses on applying AI and machine learning to molecular design challenges.

This position is one of several industrial PhD roles funded by the DDLS program, which supports training in four strategic areas: cell and molecular biology, evolution and biodiversity, precision medicine and diagnostics, and epidemiology and biology of infection. Together, we are announcing this position for a DDLS PhD student to join our teams, working in data-driven cell and molecular biology. Data-driven cell and molecular biology covers research that fundamentally transforms our knowledge about how cells function by peering into their molecular components in time and space, from single molecules to native tissue environments.

The project: The industrial PhD student will develop AI and machine learning models to predict drug metabolism, a critical area influencing drug efficacy and safety. The project addresses a major bottleneck in drug discovery-metabolite identification, which is traditionally time- and resource-intensive. By leveraging deep learning, generative AI, and molecular modeling, the student will contribute to creating faster, more accurate predictive tools.

The student will work closely with Dr. Filip Miljkovi? (Associate Principal AI Scientist) and Dr. Susanne Winiwarter (Principal Scientist) at AstraZeneca, and Dr. Rocío Mercado Oropeza (Assistant Professor) at Chalmers, within a cross-functional and dynamic research environment. This is a unique opportunity to shape the future of data-driven drug discovery at the intersection of computational chemistry, AI, and systems biology.

Essential skills/experience

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We welcome applications from highly motivated candidates with a Master of Science degree (or equivalent, 240 ECTS) in Computer Science, Chemistry, Life Sciences, or a related field.
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Strong programming skills in Python
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Understanding of basic chemistry and biology concepts
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Experience in deep learning frameworks
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Excellent communication skills in English (oral and written)

Desirable skills/experience

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Experience in generative AI or molecular modeling
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Prior research or industrial exposure
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Ability to work in a multidisciplinary and collaborative environment

If you're excited by the possibility of joining a program that merges AI and pharmaceutical innovation, apply no later than April 24, 2025. We look forward to your application! Visa mindre

We have an ambitious vision -to become a digital and data-led enterprise that disrupts the entire pharma industry. To get there we need outstanding people, and we now have an opportunity for development within our IT BA team-so if you've got a passion for IT and business improvements, this is the place!

Come join us for a 12 month temporary contract as an IT Business Analyst in Gothenburg.

At Operations IT we are driven by bringing value for our patients by developing smart solutions with tomorrow's technology - here our day job is results-oriented and global - with many ways to develop as an individual. Our team within Operations IT, the PT&D Capability, is working together with the Pharmaceutical Development & Technology business area to make sure they have the best IT solutions to support their business needs.

What you'll do

This position primarily focuses on Business Analysis while incorporating elements of Business Partnering. As a Business Analyst you will work in the AI Powered Drug Development Program (AIPDD), which is a program for E2E Drug Development connecting data sources, digital simulations, and digital twins, enabled by data retrieval, summarization and content generation. And Exploiting Generative AI Patterns as in Assistants for information interrogations and content generation.

As a Business Partner you will be aligned to the Pharmaceutical Technology & Development (PT&D) business area and work closely with a Senior IT Business Partner in the early phases of new demands as well as understanding problems and driving improvement initiatives that will provide real value to the scientists in the lab.

Accountabilities:

* Understanding of business needs from multiple stakeholders - applying specialist knowledge where applicable (according to the AIPDD ways of working) and improve in line with strategic goals, propose solutions through research.
* Break down and simplify business requirements for easy analysis, solution design, and decision-making to address medium risks/issues per AIPDD methods.
* Effectively communicate with stakeholders and delivery teams using interactive communication and influencing skills to ensure clear knowledge transfer.
* Lead, plan, and coordinate the delivery of assigned tasks, applying specialist business analyst knowledge.
* Requirements and design definition - identify functional and technical requirements, translation of these between IT and the business. Partnering with Architecture team, ensuring the technical solution will deliver the agreed business benefits.
* Provide thought leadership and innovation to drive enhanced performance by leading small projects aligned to AZ IT strategy.
* Collaborate with Senior ITBP for business strategy development, offering a tech perspective and translating business priorities into actionable IT initiatives that provide tangible value.
* Information Collation and Reporting: -Gather relevant data for comprehensive analysis and informed decision-making.

About you

We believe that you will succeed in this role if you operate with interactive communication as well as demonstrate inclusion and cultural sensitivity. Our people share an ambitious attitude; you'll need to be a self-starter, and independent thinker, owning solutions and striving to create new possibilities.

Key skills and experience

* Previous BA experience with domain and/or IT knowledge
* Experience eliciting Use Cases for AI enabled opportunities, including Machine Learning, Automation & Natural Language Processing
* Experienced in using business tools/techniques to design and deliver business change
* Strong verbal and written communication skills
* Ability to interpret and communicate technical information into business language and vice versa
* Previous experience of regulated/validated/GXP environment
* Skills in planning, change management and problem solving



So, what's next?

Be part of something where your work directly impacts a big purpose: to develop life-changing medicines. Join Us!

We look forward to reviewing your application. Please apply as soon as possible but no later than April 9, 2025.

Where can I find out more?

AstraZeneca Gothenburg site: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre

Are you a leader who possesses expertise in, and passion for, Managing Projects? Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines? If so, you might be our next Director, R&D IT - Data, Analytics & AI, Project Management.

Come join us at our vibrant site in Gothenburg, Sweden where more than 50 nationalities work together under one roof!

ABOUT OUR IT TEAM

R&D IT's vision is to deliver the best science IT capabilities in biopharma, which we define as agile, responsive and fit-for-future. Our goal is to engage with our stakeholders as a strategic partner in delivering life-changing medicines to our patients. The desired effect of your role is to take accountability as a leader for delivering a 'Best in Class' IT experience within R&D IT.

Delivering the portfolio of projects and services needs people with hybrid skill sets covering technical, analytical, project management, service management and business analysis skills, combined with an excellent knowledge of finance as well as product and portfolio strategy processes. Our project managers lead or contribute to a range of projects including IT development, data management, analytics, AI, machine learning, business transformation and more. Our projects deploy a range of technologies including internal custom built solutions, packaged software, ERP solutions, Software as a Service as well as Cloud based solutions and BI tools.

ABOUT THE ROLE

The Director of Project Management leads technology and/or business transformation projects/programs within R&D IT's Data, Analytics & AI team. This team is responsible for building scale data and AI solutions that accelerate research and development from target discovery to delivery to the patient - and everything in between.

The role will be in the Augmented Design-Make-Test and Analyse (A-DMTA) team, which sits at the heart of our Early Drug Discovery initiatives. This award-winning platform has invested heavily in building industry-leading, drug discovery solutions, integrating AI-solutions into scientists everyday work.

The role ensures that platform's deliveries align to Drug Discovery's vision and business strategy, and that capabilities to enable novel science and accelerate our early drug candidate pipeline is delivered to the customer as a result. Having a strong partnership with the science functions and wider IT capabilities, driving the demand for the solution is critical to success in this role.

The Director of Project Management is accountable for ensuring solutions solve key drug discovery needs in an integrated and simple manner, exploiting existing assets where feasible, while minimizing the long-term total cost of ownership. The role must also ensure that delivery occurs with a sense of urgency and can be completed within the approved program budget and schedule commitments; continuously assessing risk and balancing the need for flexibility and agility with conformance to standard methods and tools is a core part of the role.

The role is also responsible for the smooth and controlled running of the platform, deploying good planning, financial, resource and risk management practices across all of its products and services.

Focus areas include stakeholder management across science functions, IT, and vendor partners, risk management and delivery of value. This role is also required to collaborate with others in Program and Project Management, and drive development of the project / program management capability across IT in a tangible and measurable way.



Education, Qualifications, Skills and Experience

* Technical, Science or Business degree or equivalent years of experience
* Delivery of complex data, analytics & AI projects in a Research & Development context.
* At least 10 years of Project Management experience, ideally in a Pharmaceutical IT environment
* Skilled at working in a global organization and across cultural boundaries
* Experience in Agile Project Management
* Demonstrated skills interacting with Senior Leaders
* Experience leading large projects / programs
* Experience working with third party suppliers
* Experience working in a highly regulated environment
* Excellent relationship management, and influencing skills
* An entrepreneurial mindset and the proven ability to shape innovative solutions
* Well-developed organizational, interpersonal, written, and verbal communication skills

Desirable Requirements:

* Program/Project Management certifications preferred (Prince, PMP, MSP, Agile - Scrum, SAFe)
* Experience of working with software development teams and data scientists/informaticians.

Technology at AstraZeneca is a home for purposeful disruptors. Apply now but no later than April 13th to learn more about this exciting opportunity with a world-renowned pharmaceutical brand.



WHY JOIN US?

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies.

At AstraZeneca we're dedicated to being a Great Place to Work. We are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. We're on an exciting journey to pioneer the future of healthcare.

Help to shape our journey towards becoming a tech-enabled enterprise. Encouraged to look to the future, think strategically and innovate, we influence progress today. We are constantly introducing new solutions and technology through on our quest to grow through innovation. We love it here because put simply, we make a meaningful impact. Visa mindre

Are you passionate about the potential of data to transform the future of healthcare? Do you have the drive to pioneer strategic initiatives that ensure the highest standards of data quality and governance?

At AstraZeneca, we believe that data is the lifeblood of innovation. We are on a mission to harness the power of data to drive groundbreaking solutions that improve patients' lives across the globe.

Join us as a Data Strategy and Governance Lead at AstraZeneca´s vibrant site in Gothenburg, Sweden. Here you will play a pivotal role in defining and implementing strategies that enhance the FAIRness, interoperability, and governance of our data products. You will play a pivotal role in shaping our data future by translating policies into actionable strategies, enabling seamless access and utilization of data in R&D.

R&D IT's vision is to deliver the best science IT capabilities in biopharma, which we define as agile, responsive and fit-for-future. Our goal is to engage with our stakeholders as a strategic partner in delivering life-changing medicines to our patients.

Your Impact: In this role, you will foster an environment that empowers scientific and technological breakthroughs. You will collaborate with a diverse team of data engineers, data scientists, and IT specialists to influence policies, drive standard adoption, and advocate for data excellence across R&D. Your leadership will strengthen our data foundations, support GenAI, and ensure data quality, security, and accessibility.

Key Responsibilities:

* Lead strategic initiatives to enhance the FAIRness of AstraZeneca's data products.
* Translate and implement policies and standards into practical guidance for R&D IT solutions.
* Drive adoption of best practices across R&D IT engineering teams to enhance data quality.
* Champion data interoperability and advocate for Master Data Management and Controlled Vocabularies.
* Collaborate with the Data Office to refine data processes and reduce time-to-data access.
* Represent R&D IT across various organizations, coordinating Information Architecture and Data Modelling activities.
* Organize events and campaigns to promote data governance initiatives within R&D.

What You Bring:

* Data Expertise: Extensive experience in data-centric roles such as Data Analyst, Data Engineer, or Data Product Owner.
* Technical Skills: Proficiency in , Python, Excel, and visualization tools like Power BI.
* Governance Knowledge: Deep understanding of Data Governance and Compliance Standards.
* Leadership & Communication: Strong communication skills with the ability to build relationships, facilitate workshops, and drive consensus across multiple stakeholders.

So, what's next!

Embark on a journey where your data strategy and governance expertise directly influence innovation and enhance patient outcomes globally. Apply now but no later than April 20th to lead advancements in data strategy at AstraZeneca!

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey.

Where can I find out more?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre

Embark on a significant journey where your expertise in high-performance computing accelerates scientific discovery and impacts patient outcomes worldwide.

We are currently seeking a passionate, HPC engineer to join AstraZeneca´s vibrant site in Gothenburg, Sweden. The ideal candidate will have extensive hands-on experience making an impact with HPC technology, delivering HPC services to a high quality, and able to relate to the scientific community and work closely with users to make the best use of research computing services.

About the Role:

At AstraZeneca, our Research Data & Analytics Team is at the cutting edge of transforming how we discover and develop medicine. As an HPC Engineer within the Scientific Computing Platform, you'll be crucial in delivering HPC services and solutions that drive progress in computational chemistry, imaging, multi-OMICs, AI and more. We're combining modern HPC with leading DevOps and cloud-native technologies to push the boundaries of biopharmaceutical research.

The HPC landscape is continually evolving. You will need the skills to help build and operate industry-leading capabilities, including application build frameworks, containerized applications and cloud software-as-a-service. Automated deployment is a key feature and you will need to be comfortable with DevOps processes and delivering consistency through automation and infrastructure-as-code.



Your Impact:

Be part of a global team where your skills in high-performance computing empower innovative scientific solutions. Engage and collaborate with researchers and engineers to optimize workflows and deploy HPC capabilities that facilitate new discoveries. Your contribution will directly enhance the development of innovative medicines, improving patient outcomes globally.

Key Responsibilities:

* Develop and operate cutting-edge research computing services and applications
* Adopt Site Reliability Engineering principles to manage end-to-end HPC service operations, monitoring, and incident response
* Optimize and solve complex technical problems in the HPC infrastructure, collaborating closely with scientific users to enhance system utilization

What You Bring:

* Proficiency in Linux environments for administration and programming
* Solid skills in Python programming and bash scripting
* Highly customer-focused, with the ability to communicate complex IT concepts to non-experts
* Experience in working within a DevOps team using agile methodologies

Desired Skills and Expertise:

* Background in a scientific field or experience with computationally intensive scientific data analysis
* Experience in large-scale HPC environments, parallel filesystems, and with tools such as SLURM and OpenStack
* Familiarity with configuration automation, software distribution frameworks, and cloud deployment, especially AWS
* Expertise in AI/ML tools, parallel programming, and containerization technologies
* Understanding of domain-specific applications like bioinformatics tools, simulation software, or high-performance data visualisation packages

Join AstraZeneca and play a pivotal role in advancing HPC technology to accelerate scientific breakthroughs.

Apply now but no later than 10th of April to be a leader in HPC innovation at AstraZeneca!



ABOUT ASTRAZENECA

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energised and rewarded for their ideas and creativity.

Where can I find out more?

AstraZeneca Gothenburg site: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html

Life in Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.htm Visa mindre