Lediga jobb Hays AB i Göteborg

Type of employment: ContractWork location: Göteborg, Sweden
Start Date: ideally 2026-03-30
End Date: estimated 2026-05-29
Ways of working: on-site
Workload Allocation: 100%
Language: fluent English

We are looking for an experienced SAP PP & ePPDS Consultant to support and lead SAP Production Planning and embedded Production Planning and Detailed Scheduling initiatives. The role involves close collaboration with business stakeholders, hands-on system configuration, and end?to?end delivery of ePPDS solutions.

Key Responsibilities

* Lead and conduct customer workshops to demonstrate SAP ePPDS capabilities and best practices
* Analyze and translate business requirements into solution design
* Perform system configuration and master data setup for SAP PP and ePPDS
* Support and execute user training, process testing, and validation of all ePPDS processes
* Act as a key point of contact, handling communication with customers and project stakeholders
* Support adoption and usage of SAP Fiori applications related to planning and scheduling

Required Experience & Skills

* 10+ years of experience in SAP Production Planning (SAP PP)
* 5+ years of hands-on experience with Production Planning and Detailed Scheduling and 3 years with ePPDS
* Strong expertise in SAP PP module and advanced planning concepts
* Proven experience delivering end?to?end ePPDS implementations
* Experience working directly with customers in workshop facilitation and requirement gathering
* Solid understanding of SAP Fiori applications
* Strong communication skills and experience working with multiple stakeholders in complex project environments

Nice to Have

* Experience in large or complex SAP transformation projects
* Ability to work independently and take ownership of solution delivery

As part of the recruitment process, the client will conduct background checks on candidates who progress to later stages.

If this consultancy opportunity aligns with your experience, please click 'apply now' and submit your updated CV, clearly highlighting your expertise in the must-have competencies required for the role. We look forward to receiving your application and speaking with you as soon as possible. Visa mindre

Senior Research Scientist - Cell model and Assay development - 12 months assignment - AstraZeneca

Imagine a future where a diagnosis of a severe genetic disease is no longer terrifying because effective medicines can cure them. At AstraZeneca, we are turning this vision into reality through pioneering work in genome editing and precision medicine. Join us in this effort!

Our Genome Engineering Team in Gothenburg, Sweden focusses on developing treatment for Rare Diseases. We continually push the boundaries of science to expand the limits of scientific research to better understand rare diseases, discover new life-changing treatments and deliver medicines to patients.

As a Senior Research Scientist, you will be a key member of the Genome Engineering Department. You will join our international team that develops novel genome engineering technologies and applies these breakthroughs to generate innovative gene therapies. We provide a stimulating environment with state-of-the-art facilities where you can transform cutting-edge genome engineering tools into effective and safe medicines.

What will you do:

In this laboratory-based role, you will leverage your scientific expertise in genome engineering and innovative thinking to develop novel tools and applications that can lead to breakthrough therapies. As a key member of cross-functional project teams, you will develop and evaluate genome editing strategies for specific disease projects. Accountabilities will include innovative optimisation of genome engineering technologies to facilitate effective gene editing in target cell & tissue types, developing relevant assays, analysing gene editing outcomes, documenting, interpreting, and communicating results to appropriate partners.

Your accountabilities will include:

* Establishing and maintaining disease cell models using immortalised or iPSC cell lines
* Establishing and running cellular and biochemical assays to evaluate efficacy of therapeutic genome editing approaches in disease models
* Documenting, interpreting and communicating results to stakeholders and partners

Why AstraZeneca?

If you are passionate about translating scientific advances into real next generation medicines, AstraZeneca is the right place for you. Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

About Hays

Hays is a global recruitment company with extensive experience in matching the right skills with the right assignments. As a consultant with us, you become part of our network and gain access to exciting assignments at leading companies. Visa mindre

Scientist In Vitro Immunology - 8 months assignment - AstraZeneca - Starting in March

Join the Bioscience Immunology team within Research and Early Development, Respiratory & Immunology. You will support in vitro studies, and ex vivo analyses on mouse cells, focusing on inflammatory and autoimmune diseases. Respiratory & Immunology is one of AstraZeneca's core therapy areas, aiming to understand, treat, modify, and ultimately cure respiratory and autoimmune diseases.

What you will do:
* Plan and execute experiments: Design, perform, and analyse in vitro and ex vivo studies to advance drug discovery projects and generate publishable insights.
* Contribute scientifically: Engage in study design discussions and data interpretation; present findings, rationale, and recommendations.

Accountability:
* Hands-on work: Conduct in vitro and ex vivo analyses from rodent studies alongside a team of committed scientists.
* Data responsibility: Uphold the highest standards of data integrity, quality control, and archiving.
* Communication: Evaluate and interpret primary data; write reports and summaries; present in team and project meetings.

Why AstraZeneca?
At AstraZeneca, we are driven by our desire to understand and reveal new insights. We are free from fear of failure, free to ask the right questions, make bold decisions, and dig deep into the biology of complex diseases. We are committed to making an impact on patients' lives by improving patient access to healthcare globally. Our values guide everything we do at AstraZeneca. They power our belief in What Science Can Do - a belief in its potential to redefine what's possible.

About Hays
Hays is a global recruitment company with extensive experience in matching the right skills with the right assignments. As a consultant with us, you become part of our network and gain access to exciting assignments at leading companies.

So, what's next? If this sounds like your next challenge - please don't hesitate to apply! Visa mindre

Drug Product Delivery Operator - Consultancy Assignment in Gothenburg

Are you motivated by structure, precision and contributing to life?changing clinical research? We're looking for a detail?oriented DPD Operator to support a global biopharmaceutical company committed to advancing innovative medicines. This is a unique chance to be part of a highly regulated, science?driven environment where your work will directly support clinical trials across the world.

What you will be working with

In the Drug Product Delivery (DPD) function, you will be involved in the end?to?end handling of investigational medicinal products. Your tasks play a central role in ensuring that clinical trial materials reach patients safely, correctly and on time.

You will be part of a team specialising in:

* Material Management
* Packing & Labelling
* Distribution of investigational medicinal products

This is a hands?on operational role where accuracy, documentation and compliance are essential.

Your core responsibilities:

* Receiving, handling and packing investigational medicinal products
* Ensuring full traceability of items, batches, packaging materials and labels
* Preparing and reviewing GMP?compliant documentation
* Acting as a point of contact for distribution?related study questions
* Maintaining equipment and facilities according to GMP standards
* Supporting improvement initiatives and deviation management
* Contributing to the development of internal procedures within GMP and SHE

Who we are looking for

This role suits someone who thrives in structured environments and enjoys working within established quality systems. You are analytical, solution?oriented and able to work independently while being a reliable team contributor.

Essential qualifications:

* BSc/MSc in chemistry, pharmacy, engineering, logistics or similar
* Approximately 2 years' experience in pharmaceutical development or related field
* Comfortable working in a regulated GMP environment
* Strong communication skills in English
* Experience working in complex, multicultural environments

Beneficial skills:

* Understanding of SHE and GMP requirements in R&D or manufacturing
* Knowledge of supply chain processes within pharma
* Familiarity with clinical trial materials and distribution standards

What you can expect

You will join a highly collaborative team passionate about delivering high?quality clinical trial materials. The environment is fast?paced and dynamic, offering great opportunities to grow your skills within pharmaceutical operations and regulatory frameworks.

Ready for your next step?

If this sounds like the right challenge for you, click "Apply now" to submit your CV or get in touch with us directly to learn more.

If this particular role isn't the perfect match, feel free to contact us for a confidential career discussion.

About Hays

At Hays, we connect talented professionals with opportunities that help them grow, thrive and make an impact. With deep industry expertise and a global network, we support organisations in finding the right skills - and help candidates discover roles aligned with their ambitions.

Our purpose is simple: to empower people and organisations to succeed. Whether you're seeking your next challenge or looking to strengthen your team, Hays is here to support you every step of the way. Visa mindre

Senior Scientist - NGS Molecular Biologist - 12 month assigment - AstraZeneca

Are you an experienced scientist with great expertise in Next Generation Sequencing and Molecular Biology? We have an opening suitable for you!

Right now, we are looking for a passionate and hard-working Molecular Biologist with NGS skills to join our NGS & Transcriptomics function within the Centre of Genomic Research Department at AstraZeneca in Gothenburg, as one of our group members is going on parental leave. You will contribute with your expertise in applying molecular biology and NGS to progress drug development pipelines and disease/biology understanding.

What you will do:

This is a hands-on laboratory-based role to effectively support and deliver various clinical and preclinical projects across multiple diseases, species and drug modalities.

Our team is a collaborative group, and you will engage in the supervision and mentorship of other scientists, ensuring that methods run expertly and accurately, developing and guiding the set-up of new techniques. Included in the role is also to nurture strong collaborative relationships with the project investigators, key partners, and data scientists to ensure the smooth running of projects.

In this role you will:

* Utilize prior practical laboratory experience in transcriptomics data generation with a strong emphasis on automation technologies.

* Contribute to planning and execution of projects involving new omics technologies.

* Provide experimental support to project teams.

* Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca's corporate responsibility policies.

* Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.

* Collaborate with a wide range of scientists from different backgrounds to ensure the highest quality of research.

* Develop and validate cutting edge protocols for the simplification of multiomic research.

Why AstraZeneca?

At AstraZeneca, we are driven by our desire to understand and reveal new insights. We are free from fear of failure, free to ask the right questions, make bold decisions, and dig deep into the biology of complex diseases. We are committed to making an impact on patients' lives by improving patient access to healthcare globally. Our values guide everything we do at AstraZeneca. They power our belief in What Science Can Do - a belief in its potential to redefine what's possible.

So, what's next? If this sounds like your next challenge - please don't hesitate to apply!

About Hays
Hays is a global recruitment company with extensive experience in matching the right skills with the right assignments. As a consultant with us, you become part of our network and gain access to exciting assignments at leading companies. Visa mindre

Animal Technician - AstraZeneca - Gothenburg - 6 month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:

Animal Technician

AstraZeneca is a global, innovation-driven biopharmaceutical company that focusses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. 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, energised and rewarded for their ideas and creativity.

The Animal Science and Technologies (AST) is a global department that delivers in vivo studies, animal care, and welfare that are compliant to internal standards and external regulations. Principles of the 3Rs are applied to all aspects of animal care and study conduction.

The role
*Performs daily animal husbandry tasks for rodents and pigs to ensure the highest standards of animal care & welfare.
*Responsibilities may include breeding and maintenance of transgenic mice.
*Responsibilities may include technical procedures such as collecting biological samples, weighing and administering medicines/compounds.
*Maintains daily record keeping for animals and the environment.
*Responsibilities may include routine facility operations tasks, dish and maintenance on racks and caging equipment.
*Is required to work flexibly across different areas and participate in provision of weekend and out of hours support.
*Ensures that work is performed in accordance with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. General Laboratory Standard (GLS).

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



Essential for the role:
* Experience of working with rodents and/or strong interest in animal care and welfare.
* Understand principles and concepts associated with Laboratory Animal Science (LAS), particularly on animal welfare and the 3Rs.
* "Naturbruksgymnasium" or similar education.
* Laboratory Animal education by NCLASET or other relevant Laboratory animal science - Rodents and Lagomorphs - (LAS) course. This may be optional, if the candidate proves relevant experience in animal care.

Soft skills:
*Good communication skills
*Ability to perform work independently to the required standard on a consistent basis.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Research Scientist Membrane Protein Sciences - AstraZeneca - Gothenburg - 12-month consultancy assignment

Passionate Research Scientist in Membrane Protein Science

Are you an enthusiastic scientist with skills in the field of membrane protein biology and have a passion to use your skills to contribute to the development of medicine for patients? Do you also want to join a place where our teamwork and collaborative atmosphere drives us forward? If yes, this might be the position for you!

Right now, we have an opportunity for a motivated Research Scientist to join the Membrane Protein Science Team at our vibrant AstraZeneca R&D site in Gothenburg, Sweden, for a one-year temporary position. In this role, you'll play an important part in the Discovery Biology department within the Discovery Sciences organisation.

This is a laboratory-based research position where you will apply your skills and knowledge in protein purification and recombinant protein expression, your curiosity, combined with strong team working ethics to support our early drug discovery projects. You will join our team whose remit is to deliver impactful recombinant membrane protein reagents used to power hit-finding, lead-generation, all the way to clinical candidate validation.

What you will do:
As a Research Scientist in the Membrane Protein Science Team, you will be generating tailored membrane protein reagents to support projects in all phases of the discovery process. The role involves expression screening of constructs in eukaryotic hosts, large scale expression, and purification of recombinant membrane proteins to supply bioreagents to assay development, affinity screening and structure-based drug discovery.

You will plan and conduct experimental strategies and generate, interpret and report scientific data autonomously or in collaboration with colleagues. In addition, you will contribute to advancing our capabilities in the production of recombinant membrane proteins used in early drug discovery.

Essential Requirements:
* Master's in molecular biology, Biotechnology, Biochemistry or a related field, and 2 years of relevant working experience.
* Expertise and proven knowledge of a wide range of methods and technologies applied to the expression, purification and characterisation of membrane proteins.
* Passion for experimental laboratory-based research.

Desirable:
* Experience in recombinant expression, purification, and pharmacology of GPCRs.
* Good understanding of drug discovery and how to contribute with scientific expertise within your own area of expertise to drive project progression.
* Expertise in cell culture for recombinant protein expression in eukaryotic cell types.

We also see our new colleague as a person who thinks in an unexpected way, holds enthusiasm and curiosity towards scientific questions and learning new skills. You have great laboratory skills and the ability to make scientific judgements, as well as work in a goal-oriented way. We believe that you can work in an independent way, but you also enjoy teamwork and can communicate and collaborate in a global setting with cross-functional groups.

Why AstraZeneca?
Join the team that follows the science unlike anywhere else. This is the place for curious minds. Dig deep into the biology of complex disease and uncover breakthroughs. With more than 2,800 employees from over than 70 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Supply Chain Manager - AstraZeneca - Gothenburg - 12-month consultancy assignment

Supply Chain Manager for Clinical Trial medications

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join the Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity, at the right time for every patient taking part in AstraZeneca's trials all over the world. Our goal is to never miss a patient.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

Tasks and responsibilities/The role:
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on-time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high-pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Your main responsibilities will include:
* Project manage the delivery of clinical supplies effectively and consistently, and input into the balance of costs and any risks to supply.
* Ensure effective communication with project teams and key partners across a global network.
* Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
* Take ownership of Inventory management, including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
* Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
* Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Essential requirements:
* Bachelor's Degree in a scientific or supply chain subject area - equivalent experience will be considered.
* Experience within a supply chain management environment with a holistic knowledge of end-to-end supply chain activities
* Experience of demand planning and forecasting and risk identification and management
* Experience of running projects and influencing customer demands.
* Excellent English written and verbal communication skills.
* Proficient IT skills with an ability to adapt and operate in bespoke multiple systems.

Desirables:
* Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
* Knowledge of clinical development processes relevant to the supply of clinical materials
* Lean knowledge and understanding
* Experienced in handling Quality Events (Deviations, Change Controls, Complaints)

Soft skills:
* Strong influencing, negotiating and problem-solving skills, across geographical and cultural boundaries
* Ability to adapt and operate in bespoke multiple systems.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Clinical Supply Associate - AstraZeneca - Gothenburg - 12-month consultancy assignment

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.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
The Clinical Supply Associate (CSA) supports the clinical supply management team with task-based activities to ensure high-quality and timely delivery of materials to clinical trial patients. This role is a great opportunity for someone who thrives working in an agile, vibrant and global environment.



What you'll do:
The CSA supports teams with task-based activities that include:

* Management of temperature excursion assessments affecting clinical trial material.
* Electronic document archiving and quality control.
* User Acceptance Testing of digital systems.
* Support the coordination of the purchase and delivery of External Commercial Products.
* Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
* Coordination of ID testing requests of clinical trial material.
* Documentation and coordination of product quality complaints and GXP deviations.
* Utilising Supply Chain Management systems to support agile ways of working.
* Continually improving the Clinical Supply Chain processes through visual management, problem-solving, global standardisation and process confirmation.

In this role, you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a super-user within a core role and/or leading improvement initiatives. You will work with multiple colleagues, customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GXP standards and will be personally accountable for these areas within your own work plans.



Essential for the role:
* Degree and/or Masters in a scientific discipline or supply chain management
* Proven track record of critical thinking under pressure.
* A supply chain management ambition.
* Excellent aptitude for digital systems and an active interest in GenAI.
* Thrives in a process-orientated workplace, on task-based activities and with a focus on the customer/patient.
* Team player with a structured problem-solving mindset and a focus on quality.
* Comfortable in a high-paced and agile environment.
* Excellent communication and numeracy skills.

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 are opening new ways to work, pioneering ground-breaking methods, and bringing unexpected teams together. Interested? Come and join our journey.

So, what's next?

Are you already imagining yourself joining our team? Good, because we can't wait to hear from you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Scientist Bioscience- Automation & Assays team - AstraZeneca - Göteborg - 12-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
We are now recruiting a Scientist to join the Automation & Assays team in Bioscience technology within Early Cardiovascular, Renal and Metabolism (Early CVRM) in our dynamic R&D site in Gothenburg, Sweden.

The Automation & Assay team uses advanced automation platforms for molecular biology assays to enable delivery of high-quality data to build a detailed understanding of pharmacological response and mode of action for e.g. small molecules, oligos, and antibodies as therapeutic drugs in our pipeline projects across the Cardiovascular, Renal and Metabolism disease areas.

Tasks and responsibilities/The role:
As a Scientist, you will primarily process tissue samples using cell surface protein enrichment techniques for proteomics to provide experimental support to our drug discovery programs, development and characterisation, and optimisation of new models. There will be a possibility to be part of building automated methods for sample preparation for proteomics analysis.

Responsibilities include:
* Tissue samples using cell surface protein enrichment techniques for proteomics
* Potentially take part in the assay and method development using advanced automated platforms
* Planning and execution of experiments, troubleshooting and timely reporting/presentation of data according to agreed timelines.
* Join further model development activities to support drug projects with biomarker and molecular assays for resolving mechanisms of action, target identification, and candidate drug evaluation.

Essential Requirements:
* For the Scientist role: Master's degree + 2 years of relevant experience.
* Background in Molecular Biology, Biomedical, Pharmacology, Biochemistry or a related discipline with significant practical experience.
* Extensive experience in molecular and cellular biology techniques and, in particular protein assays and sample preparation
* Independent study design, laboratory work, and data analysis
* Excellent communication skills in English, both verbal and in writing

Desirable Experiences and abilities:
* Processing of biological samples for proteomic analysis
* Potential knowledge in Proteomics
* Independent technical capability with assay development
* Experience in automation technology such as robotic liquid handler
* Proven ability in providing technical leadership and guidance to others.
* Experience of the pharmaceutical industry

Soft skills:
* Effectively communicate and collaborate in a matrix team setting to implement technical solutions
* Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
* Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

Start date: 15/8 2025

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!

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

DPD IT/Operational Technology Engineer - AstraZeneca - Gothenburg - 7-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.
AstraZeneca is also a leading pharmaceutical company focused on developing Active Pharmaceutical Ingredients (API) with advanced technologies. The Gothenburg facility employs digital solutions and automation to enhance production efficiencies.

The arena:
The IT/OT Engineer will bridge the gap between IT and Operational Technology(equipment) in the manufacturing facility. Key responsibilities include maintaining IT systems that support business operations and manufacturing, ensuring system integrity and security, troubleshooting IT-related issues, and collaborating with various stakeholders to ensure compliance with industry standards.

Tasks and responsibilities/The role:
1. IT Infrastructure Management:
Ensure the performance and availability of IT systems.
2. OT System Support:
Align IT support with production needs.
Proactively address IT-related issues affecting manufacturing.
3. Cybersecurity Management:
Implement cybersecurity measures for IT and OT systems.
Staff training on security.
4. Data Integration & Management:
Ensure smooth data flow between IT and OT systems.
Develop interfaces for real-time data exchange.
5. System Administration & Troubleshooting:
Resolve IT incidents impacting operational efficiency.
Collaborate with vendors for advanced issues.
6. Vendor and Stakeholder Management:
Manage vendor relationships and service compliance.
Coordinate IT/OT project goals with internal teams.
7. Compliance and Best Practices:
Maintain GxP compliance and thorough documentation.
Lead system audits and validations.
8. Continuous Improvement & Innovation:
Evaluate and implement new IT/OT technologies.
Mentor junior staff and lead innovation projects.

Benefits:
* Opportunities for continuous professional development and training.

Performance Indicators:
* Maintain 99.9% uptime of IT/OT critical systems.
* Ensure rapid incident response and 100% compliance with regulations.
* Achieve high satisfaction ratings from stakeholders.

Core systems and equipment:
* High Bay Warehouse system - LAGE
* Clinical supply planning and execution System - SmartSupplies.
* Building Monitor System - EMIL
* Scanners and container label printers
* Decommissioning system - Verilite
* Label Printers with servers
* GMP Lab Computers

Essential requirements:
* Education: Bachelor's in Computer Science or related field; OT/Cybersecurity certifications preferred.
* Experience: 5+ years in IT with 2+ years in OT, especially in pharmaceutical manufacturing
* Experience with systems like SAP S4/HANA
* Experience in Power BI, Power Automate, MS Lists.
* Skills: Strong knowledge of IT/OT convergence, excellent problem-solving abilities, and understanding of cybersecurity best practices.
* GMP knowledge ideally or experience from highly regulated industries.

Soft skills/Personal Attributes:
Effective communication, multitasking, attention to detail, and commitment to excellence.

AstraZeneca is one of the world's most exciting biopharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Research Scientist - NGS based Proteomics - AstraZeneca - Gothenburg - 12-month consultancy assignment

At AstraZeneca, our achievements stem from scientific excellence. Our innovative work thrives on collaboration, ensuring that every member of our team understands how their role contributes to our broader mission of showcasing the power of science.
The NGS/Transcriptomics team is a dynamic group dedicated to advancing "omics" technologies and methodologies. Our goal is to generate insightful data that enhances our understanding of drug pharmacology, target mechanisms, model systems, patients, and diseases, aligning closely with AstraZeneca's strategy for Growth through Innovation.
We are seeking a Research Scientist with a background in molecular biology laboratory practices. The ideal candidate will possess exceptional teamwork skills and a history of collaborative success to drive scientific excellence and deliver robust results for our research projects.

Are you driven to push the boundaries of science? Do you want to contribute directly to AZ's innovative growth strategy? If yes, we invite you to join us at our R&D facility in Gothenburg, Sweden!

Main Duties and Responsibilities:
This role is for a lab-based Research Scientist with knowledge and experience in transcriptomics / proteomics. This is a hands-on laboratory-based role with a focus on effective delivery to support various clinical and preclinical projects across multiple diseases, species and drug modalities.

In this role you will:
* Utilise prior practical laboratory experience in molecular biology.
* Contribute to planning and execution of projects involving new omics technologies.
* Implement innovative processes developed by the NGS Tx team.
* Maintain laboratory processes and equipment rigorously.
* Provide experimental support to fellow team members, fostering a collaborative environment.
* Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca's corporate responsibility policies.
* Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.
* Be collaborative with a wide range of scientists of different backgrounds to ensure the highest quality of research.
* Implement cutting-edge protocols for the simplification and dissection of a multiomic environment.

Essential for the role:
* B.Sc. degree or higher in a relevant scientific discipline
* Excellent practical and theoretical knowledge and understanding of molecular biology techniques.
* Hands-on experience with at least one Next Generation Sequencing / Transcriptomics / Proteomics technology (NGS-based proteomics technology, RNA-seq, DNA-Seq, Genotyping methodologies, mass spectrometry).
* Familiarity with all aspects of the research process, from hypothesis generation to experimental execution, including sample preparation, data generation, and analysis.
* Excellent organisational and communication skills.

Desired qualifications:
* Research experience in Pharma/Biotech, medical, or academic environments.
* Experience in high-throughput workflows, including the integration of automation in routine laboratory practices.
* A record of high-quality peer-reviewed publications or scientific presentations.
* Experience in statistics, quantitative data analysis, data mining, and familiarity with LIMS (Laboratory Information Management Systems).



Start date: 2nd June

If you are interested, apply now!

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country where the role is advertised. Visa mindre

Scientist in Advanced Drug Delivery - AstraZeneca - Gothenburg - 7-month consultancy assignment

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients 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.

Pharmaceutical Sciences at AstraZeneca deliver 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. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca's clinical pipeline. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA-based therapeutics across AstraZeneca's therapy areas.
We are now recruiting a talented and motivated Scientist in the formulation area to join our New Modality Preformulation team within the Advanced Drug Delivery (ADD) function in Gothenburg, Sweden for a parental leave cover.

What You'll do
This is an exciting role where you will act as a key member of various project teams and provide your technical and scientific expertise into formulation design of biomacromolecules within the new modality area. As a Scientist, you will support drug projects from a formulation perspective in the discovery phase of the drug development process, working from target identification to candidate drug nomination. The role covers the development and characterisation of formulations of oligonucleotides of high complexity. You will support drug projects within your own function in the preclinical phase, and you will serve as a member of the cross-functional drug development project teams, representing your function and scientific area. You will work in close collaboration with formulation scientists, analytical chemists as well as biopharmaceutics experts in Gothenburg, Sweden, but also with colleagues in Cambridge, UK and Waltham, US.

Essential for the role:
* Masters or PhD degree in relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry, Biotechnology or Pharmacy)
* Previous experience of working with biomacromolecules (e.g. RNA, proteins or peptides) or formulations of small molecules.
* Ability to work independently in a laboratory setting.

Desirables:
* Industrial experience in a pharmaceutical environment.

Soft skill:
* Scientific interest in exploratory formulation/characterisation work related to complex molecules, delivery systems and new technologies.
* Ability and desire/willingness to effectively communicate, network and build collaborative relationships with partners across disciplines and cultures, internally and externally, and independently lead and influence projects.

If your passion is science & technology, and you want to be part of a team that has a positive impact on patients' lives, then there's no better place to be. With us there are many opportunities to develop yourself and your career. From our diverse portfolio and teamwork to our cutting-edge innovations - it's a place for lifelong learning.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Analytical Scientist - AstraZeneca - Gothenburg - 8.5-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energised and rewarded for their ideas and creativity. At AstraZeneca, we set pride to drive development in a sustainable way, in all areas of our business, from influencing our suppliers through development to commercial products.

Tasks and responsibilities/The role:
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us to determine the quality attributes during the development of the formulations. The work includes analytical testing, documentation, and attending and presenting in project team meetings. The role is primarily laboratory-based.



Requirements:
* BSc or MSc typically from pharmaceutics, chemistry, or analytical science, but also other disciplines with relevant skills.
* Good knowledge of written and spoken Swedish and/or English is necessary.
* Scientific knowledge within analytical science,
* Laboratory experience including working with computerised systems and chromatography techniques (e.g. UPLC) for detection of small molecules.

Desirables:
* Experience of working within the pharmaceutical industry, this will be an advantage.
* Well-organised, analytical, flexible and accurate.
* Good team working skills are also important, together with the ability to operate independently.
* Good communication skills linked to the ability to work to tight timelines are highly valued.
* If you have experience of working in a GMP environment or worked in AstraZeneca or the pharmaceutical industry, this will be an advantage.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Associate Director Site Quality - AstraZeneca - Gothenburg - 12-month consultancy assignment

Associate Director Validation, site Quality

Join us in our Site Quality Team! We provide Quality oversight in the development of investigational products and have the responsibility for Licence to Operate at our development site and play an important part in the commercialisation of new medicines. Development Quality is a Global group, with teams located in Gothenburg (Sweden), Macclesfield, (UK) and Durham (North Carolina, US). With a portfolio encompassing both small and large molecules, combination products and ground breaking technologies you will be a part of providing novel life-changing medicines to our patients around the globe.

Are you ready to take the lead in ensuring patient safety and maintaining License to Operate across our Development functions? As an Associate Director in Site Quality, you will be the prime source for quality/compliance advise on validation activities and provide quality leadership to Development functions. You will interpret AZ regulatory and GMP standards into appropriate quality standards and provide guidance to ensure AstraZeneca and Regulatory requirements are met. The role requires independent operation, risk management and lean skills, and decision-making against a background of varying regulations and standards. Your responsibility will extend to internal assets and GMP compliance decisions, having a major impact on AZ's business.

Your role
As an Associate Director, you will develop and maintain in-depth knowledge of the quality regulations and guidelines applicable to your area. You will mentor and support junior colleagues, build strong customer relationships, and participate in GxP audits/initiatives. You will also be responsible for developing and approving GMP documentation and QA risk assessments, providing Quality input into business improvement projects, and be part of external Regulatory Authority GMP inspections. You will work closely with the leadership teams of our customers to set strategic direction for quality within that area, maintaining quality oversight and driving continuous improvement.
Most appreciated in the role is the ability to lead projects, to improve processes or ways of working and support different functions with your subject-matter expert knowledge. Working in a development environment makes your role versified and enables lifelong learning in everyday tasks.

Essential for the role:
* Appropriate scientific degree with extensive experience (5-10 years) of working with validation, in a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation
* Extensive experience from working with all types of validation including, equipment, automation and IT systems.
* A broad and comprehensive understanding of Quality Systems and GMP and good knowledge and reputation in the QA arena and specifically in GMP matters
* A comprehensive understanding of the pharmaceutical/drug development process is essential. A detailed scientific understanding of the Product types being supported is desirable
* Experienced of leading projects, making decisions, acting courageously and communicating with conviction and inspiration and in building excellent relationships both internally and with external suppliers or service providers
* Understanding of Supply Chain processes is desirable

Soft skills:
*You thrive when you work independently, when leading projects and take pride in structuring your day, knowing that the diverse workload can change the schedule with little notice.
* You are a problem solver who can look at solutions in a pragmatic way - coming up with creative solutions whilst still following our strict regulations.
* Excellent team working and networking skills
* Demonstrates independent judgement and uses risk management in complex situations
* Capable of making decisions, acting courageously and communicating with conviction and inspiration
* Demands excellence (sets high bar) and delivers
* A good communicator with experience of interacting effectively across interfaces

Why AstraZeneca?
At AstraZeneca, we take Quality seriously. Our work is important, valued, and at the forefront of discovery, development, and commercialisation. We are always innovating, trialing the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and driven by our ambition to go far. We are a team of ambitious people who want to achieve. We work together as a team, get our pipeline out to patients sustainably, reliably, and safely. We follow evidence to reach outcomes that benefit patients and AstraZeneca.
Make a difference! Apply now and join us in our journey to push the boundaries of science and make a real-life difference to patients.

About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centres. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Quality Advisor - AstraZeneca - Gothenburg - 12-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team.
AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

We have an exciting opportunity for a 12-month temporary assignment as Quality Advisor in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and provide quality support to the science functions and throughout the drug development process chains.
This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products.

The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, teaming up with the pharmaceutical development functions and be involved in cross-business processes. To build strong relationships with these functions, knowing their business is key, to give support to projects and develop ways of working that build for success.

The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardise and simplify our internal processes.

Typical Accountabilities:
* Responsible for quality release of manufactured Drug Products and Investigational Medicinal Products for clinical trials
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug products.
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Minimum requirements - Education and Experience
* M.Sc. in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
* Demonstrates understanding of international quality systems regulations, concepts, and industry practices to adopt best-in-class processes
* A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous.
* Experience of interacting effectively across interfaces and collaborating internally in a good communicative way
* Fluent in written and spoken English

Required soft skills:
* Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude
* Excellent team working and networking skills and encourages team effectiveness
* A good communicator with experience of interacting effectively across interfaces and collaborating internally

About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centres. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Assoc. Princ. Scientist Bioscience - AstraZeneca - Gothenburg - 12-month consultancy assignment

We are now recruiting an Assoc. Princ. Scientist Bioscience with knowledge of in vivo experimental biology to join the Bioscience Renal in vivo team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area. The position is located at AstraZeneca's dynamic R&D site in Gothenburg, Sweden.

As Assoc. Princ. Scientist with the Bioscience department at AstraZeneca, you will be part of a vibrant team that focusses on finding new treatment options for patients with renal disease. In the in vivo team we work with various pre-clinical models and different drug modalities. You will take part in in-vivo deliveries to drive the renal pipeline. At AstraZeneca, you will work together with experts from different functions and be part of project teams.

What you'll do:
* Independently design, plan and perform high-quality in vivo experiments in preclinical models of renal disease
* Identify and implement new models/assays relevant for the renal disease area
* Analyse fluids for biomarker quantification
* Perform conceptual interpretation and presentation of generated data
* Act as Bioscience representative in assigned projects
* Potentially act as new Target Champion, ie proactively identify and develop new target ideas into projects
* Deliver data, presentations, reports and regulatory documents
* Show scientific leadership in areas associated with the role - renal pathology and pathophysiology - by presenting data internally in key forums
* Ensure that your own work and work with others is performed according to appropriate safety, health and environment (SHE), quality and compliance standards, e.g. General Laboratory Standard (GLS)



Essential for the role:
* PhD in biology, physiology, pathology or medicine or other relevant areas
* Extensive hands-on experience of running in vivo experiments in rodents with experience in renal models
* Educated and certified for in vivo experimentation
* Proven publication record
* Strong oral and written communication skills. English is essential, Swedish is appreciated but is not a requirement.

Desirable for the role:
* Flexibility & independence
* Experience working with preclinical contract research organisations
* Expertise in renal physiology and/or pathology
* Experience from the Pharmaceutical industry

Why AstraZeneca?
Here we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Research Scientist Chemistry - AstraZeneca - Gothenburg - 12-month consultancy assignment

Research Scientist Chemistry, Compound Management

Are you a passionate scientist, eager to join a company at the forefront of sample management technologies? Would you like to contribute to the continuous improvement of life-changing projects? Perfect, we have a new challenge for you!

We are looking for a motivated and engaged team member for our Compound Management team at our vibrant R&D site at AstraZeneca in Gothenburg, Sweden.

In this role you will be responsible for the storage and timely supply of compounds to AstraZeneca's drug discovery projects. Highly automated liquid handling systems will be employed to supply molecules to AstraZeneca scientists and partner organisations. You will be a part of the Discovery Sciences organisation, operating within a first-class scientific environment to support drug discovery across each of AstraZeneca's Therapeutic Areas.

Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.

What you will do:
In this position, you will get the opportunity to work in a dynamic and enthusiastic environment, whilst delivering critical support to all phases of drug discovery projects and working with a broad range of chemical modalities. You will be supporting projects by providing compounds in the requested format - assay ready plates, serially diluted mother plates, formulations and solids. Bringing in new capabilities and building new processes are core activities within our group, performed in a cross-functional collaboration setting with the drug discovery projects.

You are expected to act upon day-to-day issues that occur whilst processing samples and run Compound Management development projects to ensure continuous improvement within the local team and the global department.

Examples of typical tasks:
* Designing, performing and interpreting experiments independently to investigate process improvements and evaluate new technologies.
* Working closely with internal project teams to meet drug discovery needs.
* Rapidly addressing customer queries with regards to Compound Management orders, software, processes and capabilities.
* Achieving personal scientific visibility through project contributions, internal presentations and publications.

We work collaboratively within our Compound Management team to understand the customer needs and how to add value through our experience and capabilities. To maintain this position and provide support within agreed service levels, we actively seek ways to improve our process and exploit new technologies.



Essential for the role:
* A BSc/MSc in Chemistry/Biotechnology/Chemical engineering
* Excellent communication skills and high work ethics.
* Excellent problem-solving skills and ability to identify and implement improvement activities.
* A track record of the performance of a range of practical skills, including non-routine complex tasks, to a high level.
* Passion for science, technology and innovation and understands the drug discovery process

Desirable for the role:
* Previous experience of working in a compound management role and operating integrated automation equipment like liquid handlers and scheduling software is a strong merit.
* Some experience with IT (/Python/Java coding) is an advantage but not a requirement.

Why AstraZeneca?
Here we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Business Support Coordinator - AstraZeneca - Gothenburg - 6-month consultancy assignment

At AstraZeneca, every one of our employees makes a difference in patient lives every day. Development Operations brings together all the skill groups to drive critical operational activities for early and late-stage medicine development. We have deep and specialist expertise in study and site management, data management, technical systems and processes, and in working with Contract Research Organisations and partner organisations to ensure the fast, efficient, ethical, and quality delivery of our clinical trials in countries around the world.

Reporting to the Business Support Leader, this role will focus on ensuring a seamless documentation process by coordinating and communicating with internal and external stakeholders, based globally. We are looking for an enthusiastic, driven, and flexible individual with experience of working at a senior level in a fast-paced, complex, global environment.

Your accountabilities:
* Adhere to the AstraZeneca Power of Attorney established process, including the proactive management of requests in an accurate and timely manner.
* Offer comprehensive support and guidance on the process to stakeholders, ensuring all assistance remains within the scope.
* Maintain effective communication with stakeholders on process-related matters.
* Oversee the process following general guidance to ensure business continuity, reviewing, and refining supporting guidelines as necessary.
* Work collaboratively with global colleagues to deliver a lean, consistent, and professional global support service, including knowledge sharing and training within the Business Support team.
* Plan, organise, and schedule one's workload so that all activities are completed accurately and on time while using and developing best practices.

Essential requirements for the role:
* Experience working within defined processes.
* Excellent technical skills, proficient in Adobe Sign, Microsoft PowerPoint, MS Teams, and SharePoint Online.
* Entrepreneurial thinking with respect to the use of future technologies.
* Good communication and interpersonal skills.
* Fluent English skills.
* Experience and confidence using virtual meeting technologies.
* Ability to manage multiple projects/tasks/assignments simultaneously and effectively.
* Strong customer service skills.
* A high degree of personal credibility when interfacing with organisations internal and external to AZ.
* A strong self-starter.

Desirable experience for the role:
* Experience working in a pharma or healthcare environment.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Senior Scientist Bioscience Cardiovascular - AstraZeneca - Gothenburg - 12-month consultancy assignment

Senior Scientist, In Vitro Cardiovascular Biology

Do you have expertise within in vitro cardiovascular biology and enjoy working in the lab? Would you like to apply your expertise in a global company that is accelerating innovative science and turn ideas into life-changing medicines? Join us to discover future treatment of Cardiovascular, Renal and Metabolic diseases!

At AstraZeneca, we work at the cutting edge of science to develop the ground-breaking medicines of the future - here we do things that have never been done before. We put patients first and strive to meet their unmet needs worldwide.

CVRM is one of three main therapeutic research areas within AstraZeneca. Early CVRM has a patient-centric approach for discovering novel treatments for patients with cardiovascular-, chronic kidney- and metabolic diseases and delivering candidate drugs into late-stage clinical development. In the Bioscience Cardiovascular department, we focus on identifying and validating new drug targets for treatment of patients with cardiovascular disease and heart failure, as well as evaluating pharmacological aspects, e.g. efficacy and mechanism of action, of potential new drug candidates. The in vitro team delivers key data to projects across all phases of the drug discovery and development process, and we work with different modalities such as small molecules, modified mRNA, antibodies, cell therapy, antisense oligonucleotides and peptides.

We are now recruiting a Senior Scientist with expertise in cardiovascular biology to join the Bioscience Cardiovascular in vitro team within the Cardiovascular, Renal and Metabolism (CVRM) therapeutic area at AstraZeneca in Gothenburg, Sweden.

What you'll do:
As a Senior Scientist, you will play a key role in driving science and projects within the cardiovascular area forward. This is a lab-based role where you will explore novel drug targets with key in vitro data. Collaboration is critical for successful delivery of drug projects, and you will work closely with scientists/teams from a wide range of different functions within AstraZeneca as well as with external partners and collaborators. You will work with in vitro biology using cell lines, pluripotent stem cells (PSC) and primary cardiovascular cells, along with molecular and functional biology techniques. You will have the opportunity to try novel techniques and ideas required for progressing the existing portfolio and novel science. Responsibilities include:

- Independently design, develop and run in vitro studies and assays for target identification and validation
- Work with molecular biology methods, imaging and assays for functional readouts such as contractility and cardiac metabolism
- Contribute to communications of scientific findings through publications in scientific journals and at meetings
- Proactively contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared



Essential for the role:
* PhD or master's degree in biology, pharmacology, cardiovascular disease or similar
* Strong experience in cell and molecular biology, biochemistry and relevant in vitro/ex vivo assays within the cardiovascular area
* Experience in handling and manipulating relevant PSC cells and primary human and animal cardiac cell types, including cardiomyocytes
* Excellent English communication skills, both spoken and in writing

Desirable for the role:
* Experience with cardiomyocyte biology and function in healthy and diseased systems
* Background in drug discovery and development in the pharmaceutical industry
* Background in Vivo and in Vitro



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Quality Advisor - AstraZeneca - Gothenburg - 12-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus for our Gothenburg team.

AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

We have an exciting opportunity for a 12-month temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chain.
This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products.

The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, team up with the pharmaceutical development functions and be involved in cross-business processes. To build strong relationships with these functions, knowing their business is key, to give support to projects and develop ways of working that builds for success.

The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardise and simplify our internal processes.

Typical Accountabilities:
* Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug products
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Minimum requirements - Education and Experience
* MSc in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
* Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes
* A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous
* Experience of interacting effectively across interfaces, collaborating internally in a good communicative way
* Fluent in written and spoken English

Required soft skills:
* Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude
* Excellent team working and networking skills and encourages team effectiveness
* A good communicator with experience of interacting effectively across interfaces and collaborating internally

About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Separation Scientist - AstraZeneca - Gothenburg - 6-month consultancy assignment

Separation Scientist - High Throughput & Automated Purification

Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialised separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You'll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.
We are a global, science-led BioPharmaceutical company and our innovative medicines are used by millions of patients worldwide. With our ground-breaking pipeline comes a bright future - a secure job, exciting opportunities, and varied work. You will be valued. Not only for your unique contribution, skills, and background, but because we recognise people are our greatest asset. Here we are dedicated to being a Great Place to Work.

What you will do:
As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries.

In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.

You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.

Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities for the role:
* Provide hands-on separation science support to drug discovery chemistry using state-of-the art chromatographic instrumentation
* Deliver automated analysis and purification of novel compounds using Liquid chromatography-mass spectrometry (LC-MS) and High-performance liquid chromatography (HPLC)
* Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
* Work within the team to suggest process and infrastructure improvements
* Contribute to a vibrant and entrepreneurial organisation focused on innovation & project delivery; collaborating closely with scientists across the discovery organisation

Why AstraZeneca Gothenburg?
With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, 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.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Senior Scientist in Microphysiological Systems - AstraZeneca - Gothenburg - 12 month consultancy assignment

Flow cytometry Senior Scientist in the Microphysiological Systems (MPS)

Do you have experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases!

At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs - here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for!

This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

What you'll do:
You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterisation, and optimisation of advanced cell models and flow cytometry-based assays. We'll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods.

Responsibilities include:
* Develop and execute flow cytometry-based assays for cell characterisation and functional analysis, including panel design.
* Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS.
* Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging.
* Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation.
* Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions.



Requirements for the role:
* Master's degree + 4 years of relevant experience.
* Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar.
* Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation.
* Strong hands-on cell culture experience.
* Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs).
* Independent study design, laboratory work, and data analysis.
* Data visualisation and statistical analysis.
* Strong interpersonal and communication skills in English, both verbal and written.
* Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery.

Desired for the role:
* Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures.
* Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue.
* Experience in culturing immune cells.
* Handling microfluidic chips.
* Workflow automation, e.g., robotic liquid handling.
* Experience of the pharmaceutical industry.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Scientist EPDM - AstraZeneca - Gothenburg - 6 month assignment

Hays is currently recruiting a scientist for a consultancy role for AstraZeneca.

Scientist - Early Product Development and Manufacturing

Are you ready to make a significant impact on the development of new medicines? Join us at AstraZeneca's Early Product Development and Manufacture (EPDM) unit in Gothenburg, Sweden. We are accountable for delivering a vast portfolio of early investigational medicinal products, supplying different types of clinical trial material to studies across the globe. This is your chance to explore and innovate in our dynamic environment!

This is an exciting opportunity to join our Pharmaceutical Sciences department, which is accountable for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca's therapeutic areas. The role will be offered at Scientist level.

What you will do:
As part of the EPDM manufacturing unit, you will work in a GMP (Good Manufacturing Practice) environment, contributing to the delivery of clinical results. Your role will focus on the manufacturing of drug products, with responsibilities including timely manufacture of various drug products, working with practical hands-on processes in our GMP facilities, monitoring regulatory requirements, supporting documentation activities, and driving initiatives to improve flexibility and productivity. As we are investing in innovative technology, amongst others within Continuous manufacturing, we need to expand knowledge and competence in this area. Depending on prior experience and interest, this role could be more adapted to this area.

Accountabilities include:
* Work with practical hands-on processes in our GMP facilities following manufacturing batch records and performing transactions in material management systems.
* Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
* Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
* Rapidly develop strong competence within relevant process technologies and build credibility and the ability to drive and secure product establishment, scale-up and clinical manufactures.
* Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
* Assess records and report manufacturing and validation data accurately according to GMP.
* Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
* Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Analytical Scientist - AstraZeneca - 12 month consultancy assignment - Gothenburg

We are currently recruiting two Analytical Scientists for a consultancy assignment for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energised and rewarded for their ideas and creativity. At AstraZeneca, we set pride to drive development in a sustainable way, in all areas of our business, from influencing our suppliers through development to commercial products.

Tasks and responsibilities/The role:
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us to determine the quality attributes during the development of the formulations. The work includes analytical testing, documentation, and attending and presenting at project team meetings. The role is primarily laboratory based.

Requirements:
* BSc or MSc typically from pharmaceutics, chemistry, or analytical science, but also other disciplines with relevant skills.
* Good knowledge of written and spoken Swedish and/or English is necessary.
* Scientific knowledge within analytical science.
* Laboratory experience including working with computerised systems and chromatography techniques (e.g. UPLC) for detection of small molecules.

Desirable:
* Experience from working within the pharmaceutical industry.
* Well organised, analytical, flexible and accurate.
* Good team working skills are also important, together with the ability to operate independently.
* Good communication skills linked to the ability to work to tight timelines are highly valued.
* If you have experience from working in a GMP environment or the pharmaceutical industry, this will be an advantage.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

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Operations Regulatory CMC Specialist - AstraZeneca - 7 month consultancy assignment - Gothenburg

We are currently recruiting an Operations Regulatory CMC - Specialist for a consultancy assignment for AstraZeneca.

Do you have expertise in regulatory and overall understanding of GxP requirements? Are you highly collaborative and like contributing to clear instructions and implementing process improvements? This opportunity as Processes Specialist in the Regulatory Process and Compliance team might be the right opportunity for you.

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

Global Regulatory Excellence's vision is to Leading enterprise-wide regulatory strategies, policy and delivery - so that no patient waits. In the Regulatory Process and Compliance team, we network collaboratively to enable our customer groups to operate efficient processes in a compliant manner.

What you'll do
As a Processes Specialist in the Regulatory Process and Compliance team, you will be working with the Process team members and taking responsibility for the management of assigned tasks related to procedural document management. You will act as technical writer and reviewer, and support project management to ongoing procedural document update program.
You will be accountable for executing the delivery of the authoring and lifecycle management of current procedural documents. We hope that you have the drive to establish a culture of continuous improvement, high performance, flexibility and quality, emphasising a "can do" attitude and ensuring high standards of quality in all outputs.

Other key responsibilities in this position:
* Identify opportunities for and drive the enhancement of existing processes and procedural documents
* Using understanding of regulatory processes and regulations to provide support to the regulatory process team
* Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions
* Review and verify documents and data for accuracy and completeness
* Collaborate with team members to ensure high standards of quality in all outputs
* Contribute to communication and change management activities associated with process initiatives



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

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Formulation Scientist - AstraZeneca - 12 month assignment - Gothenburg

Consultancy role for AstraZeneca.

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients 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.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
Are you an enthusiastic, innovative, and motivated Formulation Scientist seeking a unique opportunity? Join one of our small molecule formulation teams in Pharmaceutical Sciences at AstraZeneca's vibrant R&D site in Gothenburg, Sweden. Collaborate with dedicated teams and work closely with other skill experts in our common effort to drive AstraZeneca's pipeline forward.

Responsibilities
This is a lab based role where you will support project teams and provide your technical and scientific expertise into formulation development. You will develop and deliver different formulation systems for oral and parenteral use, with focus on liquid formulations, supporting projects in preclinical and clinical phase. You will also perform essential characterisation work.
This requires a tight collaboration with other internal functions and external partners to build our capabilities in drug delivery as well as engaging with customers in the development of solutions by applying a broader perspective.

You are expected to perform lab-based experimental work in accordance with project timelines, in close collaboration with other formulators, analysts, solid state and biopharmaceutical experts. The work should be documented carefully and to the right quality.

Essential requirements:
* MSc degree in a discipline relevant to formulation science, pharmaceutical technology, chemical engineering or equivalent qualifications.
* Experience in working with formulation development or similar product development, or other laboratory skills of relevance.
* Technical competence in the field of drug product formulation development for oral and/or parenteral delivery is desirable
* Good understanding of suitable quality standards and regulatory frameworks is desirable

Soft skills:
* Delivery focused with the ability to utilise scientific and innovative thinking.
* Genuine interest in experimental work and hands-on problem-solving.
* Great communication skills in English, both orally and in writing.

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. Join us at AstraZeneca, where we truly understand science and apply it every day to strengthen and grow our pipeline.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Solid State Scientist/Senior Scientist - AstraZeneca - Gothenburg

We are currently recruiting a Solid State Scientist/Senior Scientist to AstraZeneca for a 6-month assignment, with the possibility of extension.

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients 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.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
We're looking for talented and motivated solid-state scientists to join our solid state and automation team within Early Product Development and Manufacturing (EPDM) in Gothenburg.

You would join a highly collaborative team and help us deliver the solid-state science to product development within the early portfolio from discovery up to phase II.
To be successful in this role, you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
The successful applicant will become a core member of the global Solid-state skill area which is responsible for ensuring suitable physical form screening, selection and control within drug substances and products. You will get the opportunity to apply your excellent crystallography and solid-state expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of solid-state science at AstraZeneca.

Accountabilities/Responsibilities

* Deliver solid state characterisation data in our state of the art laboratory using techniques like TGA, DSC, XRPD and DVS.
* Responsible for ensuring suitable physical form screening, characterisation, form selection and control within drug substance and product.
* Drive solid state skill area in projects and work closely with analytical, formulation, and biopharmaceutics scientists to drive science and innovation.
* Plan and conduct lab-based experimental work in accordance with project timelines.
* Run and develop solid state workflows on automation equipment such as weighting robots and liquid handling systems
We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, 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.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Senior Scientist, SPR & Biophysics - Protein Science, Structural Biology and Biophysics - AstraZeneca - Gothenburg - 12 month assignment

Consultancy role for AstraZeneca

Are you a scientist with expertise and enthusiasm for applying Surface Plasmon Resonance (SPR) and other biophysical tools to uncover molecular interactions and advance drug discovery? Do you want to leverage your skills to broaden the application of SPR and related techniques in impactful drug discovery projects, while growing your career within a company that values science and transforms ideas into life-changing treatments? AstraZeneca has an exciting opportunity for you!

AstraZeneca is committed to the development of the next generation of innovative medicines. To help us with this, we are looking for a scientist with passion, expertise and experience to join our Protein Science, Structural Biology and Biophysics department as a lab-based Senior Scientist on a one-year contract basis within the Biophysics team. The team is based in our vibrant R&D site in Gothenburg, Sweden and applies biophysical technologies across a range of different modalities to support drug discovery from target validation to drug candidate. You will be part of a team of enthusiastic scientists that deliver deep technical and scientific expertise by applying molecular biophysical methods, including SPR, NMR, ITC, DSF, HDX-MS and single molecule approaches. This is a unique opportunity to contribute to the development and execution of research strategies for the discovery of new medicines - and be focused on the field of Biophysics.

What you will do:

The role of Senior Scientist is a laboratory-based position supporting the characterisation of molecular interactions in drug discovery, with a focus on Surface Plasmon Resonance (SPR) and other biophysical techniques. We are seeking a highly skilled and motivated biophysicist with deep expertise in SPR assay development, method optimisation, and screening to join our team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in biophysical techniques, particularly SPR, along with experience in protein-ligand interactions. This role is crucial in advancing our research and development projects across various therapeutic areas.

You will have significant control and influence over project direction, allowing you to shape experimental strategies and outcomes. Additionally, you will have opportunities to learn new techniques and develop your leadership skills. Working in a collaborative and innovative environment, you will engage with scientists from diverse disciplines. This position offers a unique chance for professional development in an industrial setting, helping you gain valuable experience and build a strong foundation for future career growth.

You will be responsible for designing and implementing advanced SPR assays, tailored to specific research needs, as well as larger screening activities. You will conduct intricate experiments aimed at understanding binding kinetics, affinity, and thermodynamics, ensuring accurate and precise data collection and reporting. Your expertise will be crucial in analysing SPR data, interpreting results, and integrating findings with other research data to provide comprehensive insights into drug mechanisms of action. You will collaborate closely with multidisciplinary teams, contributing to the integration of SPR and biophysical findings into broader research objectives. Additionally, you will keep abreast of the latest advancements in SPR and biophysics, continuously applying this knowledge to enhance our research capabilities.

You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward. Finally, to be successful in this role, we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal-oriented and problem-solving attitude.

Why AstraZeneca?

When we see an opportunity for change, we seize it and make it happen, because any opportunity 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 in finding new ways to work, pioneering cutting-edge methods and bringing unexpected teams together!

Does this sound like your next challenge and place to work? We look forward to your application. Visa mindre

R&D Director of Procurement - AstraZeneca - 12-month assignment - Gothenburg

Consultancy role for AstraZeneca.

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company 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!

AstraZeneca is now recruiting a Director to join R&D Procurement. This position is located at one of AstraZeneca's vibrant strategic R&D sites in Gothenburg, Sweden. AstraZeneca has a single R&D Procurement group which supports the two integrated R&D science units - Oncology and Biopharmaceuticals (Respiratory, CVRM and INA). These units have responsibility for the value chain from discovery through to late-stage development, enabling rapid acceleration of promising early-stage assets and life-cycle management programs. The R&D structure is designed to help us build on this proud legacy of scientific contribution, and ensure we are positioned to continue to translate our innovative science into even more life-changing medicines for patients.

Your role
Join our diverse community and contribute to our truly global Procurement team, which reflects the full diversity of the people we serve. In this procurement leadership role, you will be accountable for the overall management of a cluster of categories, or a complex category within R&D Procurement and it may also include managing activities of a group of Global Procurement Associate Directors. You are expected to lead, coach and develop non-direct report team members to achieve set goals. You will do this by acting as a role model for our AstraZeneca Values and Behaviours. The role reports to the Senior Director of Procurement R&D Lab Equipment, Services and Supplies. Other parts of your role:

Strategy:
Accountable for designing, and implementation of global categories that include region or market strategies to optimise business efficiency
Accountable for ongoing global category management including strategic sourcing, supplier collaboration and innovation, contract and risk management
Accountable for developing and maintaining expert knowledge of respective global supply markets, competitors and product innovations
Accountable to understand the global spend and identify ongoing opportunities to increase quality and improve value for money. Facilitate implementation of procurement change initiatives within categories to improve business performance

Business & Supplier Engagement:
Develop an extensive understanding of customer needs and the business environment and translate this into meaningful Procurement projects
Builds strong relationships with stakeholders and ensure customer satisfaction
Responsible for Category level sustainability actions, ensuring our suppliers are aligned and delivering in line with our sustainability goals
For Procurement owned suppliers accountable for all aspects of supplier relationship management
Instil the highest standards of compliance and ethics consistently across AZ

Essentials for the role
- Degree level qualification or relevant experience
- Thorough knowledge of the pharmaceutical industry (or other industry), specifically Lab equipment, services and supplies
- Expertise in at least one area of Procurement or relevant R&D experience
- Proven leadership experience
- Communication skills and ability to influence others
- Comfort with risk and ambiguous situations

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 fuel 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.

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.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

IT Manager in the Digital Marketing domain - Göteborg

IT Manager, Digital Customer Experience

Essity is a leading global hygiene and healthcare company. They are committed to improving the quality of life through high-quality hygiene and healthcare solutions. They sell their products and solutions in around 150 countries under many strong brands, including the global market leaders TENA and Tork, as well as well-known brands such as Jobst, Leukoplast, Libero, Libresse, Lotus, Nosotras, Saba, Tempo, Vinda and Zewa.

About The Role
As an IT Manager in the Digital Marketing domain, you will be reporting to the Senior IT Manager Digital Marketing and will be at the forefront of delivering and supporting a robust and comprehensive application portfolio. You will play a pivotal role in ensuring the seamless functionality and continuous improvement of digital marketing applications, contributing to the success of customer experience and brand awareness strategies. The ideal candidate will possess a deep understanding of digital marketing technologies, a proven track record in delivering and supporting web applications, and strong leadership skills.

We're looking for people who aren't afraid to challenge, innovate, experiment, and move at a fast pace.

What You Will Do

* Application Portfolio Management: Develop and execute a strategic roadmap for a product line within a digital marketing application portfolio, aligning it with business goals and marketing strategies. Evaluate, select, and implement new applications to enhance the digital marketing technology stack.
* Delivery and Implementation: Lead the planning, development, and implementation of custom-built digital marketing applications, ensuring timely and successful delivery. Collaborate with cross-functional teams, including marketing, IT, and external vendors, to achieve project objectives.
* Support and Maintenance: Establish and oversee effective support and maintenance processes for a product line in the digital marketing application portfolio. Coordinate troubleshooting efforts and resolve application-related issues to minimise downtime and disruptions.
* Team Leadership and Development: Manage a Full Stack team of IT professionals responsible for the delivery and support of digital marketing applications. Foster a culture of innovation, collaboration, and continuous improvement within the team.
* Vendor Management: Collaborate with vendors to ensure the effective delivery of application solutions and services. Negotiate contracts, manage vendor relationships, and ensure adherence to service level agreements (SLAs).
* Performance Monitoring and Optimisation: Implement monitoring tools to track the performance and efficiency of digital marketing applications. Analyse data to identify areas for optimisation and enhancement, ensuring optimal functionality.
* Compliance and Security: Ensure that digital marketing applications comply with relevant data protection regulations and industry standards. Implement security measures to safeguard application data and user information.

Who You Are

* Education and Experience: Bachelor's degree in Information Technology, Computer Science, or a related field. Master's degree is preferred. 4 years of experience in IT management, with focus on Marketing Technology and digital customer experience solutions.
* Technical Skills: Proficiency in web development technologies, e-commerce platforms, and content management systems. Familiarity with MACH architecture principles.
* Leadership and Management: Proven experience leading and managing a team of IT professionals. Strong project management and SDLC skills with a track record of delivering agile projects on time and within budget.
* Strategic Thinking: Demonstrated ability to develop and execute a strategic roadmap for digital marketing technology initiatives. Strong analytical and problem-solving skills with a strategic mindset.
* Communication Skills: Excellent written and verbal communication skills in English. Ability to communicate complex technical concepts to non-technical stakeholders.
* Collaboration and Teamwork: Ability to foster a collaborative and inclusive team environment. Proven experience collaborating with cross-functional teams to achieve common goals.
* Location and Travel: This position is offered with a hybrid working pattern (3 days in office and 2 days from home). The position is based in Munich or Gothenburg. Ability to travel is up to 15%.

What's next? If this sounds like a good opportunity to you - welcome to apply! Visa mindre

Consultancy role for AstraZeneca

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
AstraZeneca is a global, innovation-driven biopharmaceutical company that focusses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. 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, energised and rewarded for their ideas and creativity.

The Animal Science and Technologies (AST) is a global department that delivers in vivo studies, animal care, and welfare that is compliant to internal standards and external regulations. Principles of the 3Rs are applied to all aspects of animal care and study conduction.

The role:
*Performs daily animal husbandry tasks for rodents and pigs to ensure the highest standards of animal care & welfare.
*Responsibilities may include breeding and maintenance of transgenic mice.
*Responsibilities may include technical procedures such as collecting biological samples, weighing and administering medicines/compounds.
*Maintains daily record keeping for animals and the environment.
*Responsibilities may include routine facility operations tasks, dish and maintenance on racks and caging equipment.
*Is required to work flexibly across different areas and participate in provision of weekend and out of hours support.
*Ensures that work is performed in accordance with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. General Laboratory Standard (GLS).

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Consultancy role for 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.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
The role
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role, you will have interactions with internal and external stakeholders.

Typical Accountabilities:

* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials.
* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities.
* Providing proactive quality advice to support the development, implementation, and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards.
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects.
* Provide appropriate Quality Assurance input to business improvement projects.
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Requirements:

* Degree in pharmacy or engineering (specialising in Pharmaceuticals)
* 3 years' experience of working within a pharmaceutical GMP environment.
* Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP).
* Experience of documentation, deviations, changes, and other quality and compliance decisions in the development projects.
* Fluent in written and spoken English.

Desirable:
* Experience preferably within a pharmaceutical manufacturing organisation.
* Understanding of Project Management processes.
* Good team work and networking skills.
* Capable of making effective decisions.
* Demonstrate drive and energy in the role to make a difference.
* Demonstrate a high degree of personal credibility.
* Comprehensive understanding of the pharmaceutical/drug development process.
* Good communicator with experience of interacting effectively across interfaces.



What you need to do now

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Consultancy role for AstraZeneca

Inhalation Product Development (IPD) at AstraZeneca is a multinational organisation that combines decades of experience in inhalation technology, whether it is nebulisation, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

We are now seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterisation of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterisation of inhaled products.

This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, documenting your experiments carefully and to the right quality, utilising both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.

To be successful in this role you will need an analytical background combined with excellent communication skills and the ability to engage and collaborate cross-functionally. We are looking for a candidate that possesses a fair understanding of the overall drug development process and has an enthusiasm for laboratory-based work as well as solving technical challenges and problems.

Essential qualifications for the role:

* BSc or MSc degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology.).
* Scientific knowledge within analytical sciences and technically skilled with analytical separation techniques such as liquid chromatography (UPLC).
* Strong scientific interest and ambition to develop yourself in the analytical sciences area as well as learning analytical techniques used for inhaled products.
* Excellent communication skills in English, both oral and written.
* Understanding the principles and applications of GMP.

Desirable skills:

* Experience in aerosol characterisation techniques used for inhaled products, such as impactor analysis.
* Experience of working in a GMP environment.
* Experience with method development and validation.
* Experience with solving technical challenges and problems.
* Experience of analysis of small molecules.



What you need to do now

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Consultancy role for AstraZeneca for a 6-month assignment.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients 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.

Inhalation Product Development (IPD) at AstraZeneca is a multinational organisation that combines decades of experience in inhalation technology, whether it is nebulisation, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

Tasks and responsibilities:
We are seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterisation of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterisation of both small and large molecules.
Responsibilities:
This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, utilising both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.
You will apply your analytical expertise with large and/or small molecules to specific drug projects, contributing to the analytical development and strategy within the inhaled project.
You will be contributing significantly to Chemistry, Manufacturing, Control (CMC) aspects of the project, working closely with formulation scientists, device engineers, biopharmaceuticals and process engineers at IPD Gothenburg as well as globally with colleagues at IPD North Carolina.
To be successful in this role, you will need a strong analytical background in working with different types of molecules combined with excellent communication skills and the ability to engage and collaborate cross-functionally. We are looking for a candidate that possesses a fair understanding of the overall drug development process and has an enthusiasm for laboratory-based work as well as solving technical challenges and problems.

Essential requirements:
-Degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology). (PhD or Bsc/Msc with extensive experience).
-Experience with analytical separation techniques such as liquid chromatography (UPLC) for large and/or small molecules. Experience with large molecules would also be beneficial. Proficiency in method development and validation of analytical methods. Experience with analytical methodologies for oligonucleotides, peptide and protein characterisation (e.g., capillary electrophoresis, ion-exchange chromatography, ELISA, SDS-PAGE) is highly desirable.
-Strong data analysis skills, with the ability to interpret results and communicate findings effectively to stakeholders, along with a proven ability to solve technical challenges and problems. Insights into the use of statistical analysis software would be great. Familiarity with working and communicating within a global, cross-functional project environment is desirable. Understanding of analytical development work and CMC delivery projects.
Experience working in a GMP environment and knowledge of corresponding instrument/equipment maintenance procedures as well as knowledge of the overall drug development process from discovery through to launch would be beneficial. Experience in aerosol characterisation techniques used for inhaled products, such as impactor analysis, would be a bonus.
-Excellent communication skills in English, both oral and written.

AstraZeneca is one of the world's most exciting biopharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

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This is a consultancy role for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consists of 7 teams spread across Sweden, UK and the US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.

What you'll do:
As a Senior Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give you the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that can rapidly become an integrated project member and deliver key data.

We will rely on you to:
* Execute in vitro/ex vivo experiments according to study plans
* Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
* Effectively communicate results to other members of the project, team or to departments as required
* Be an effective team member in supporting projects to meet their objectives
* To conduct where appropriate, in parallel more than one area of work to agreed timelines
* Possess a range of practical skills and demonstrate flexibility within and across teams

Essential requirements:
-A relevant science degree (PhD) (e.g. Molecular/Cell Biology, Pharmacy, Biotechnology)
-Practical experience running in vitro assays and cell culturing
-Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
-Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be beneficial.
Experience in lung research is desirable
- Excellent written and oral communication skills in English is a must

Soft skills:
You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player, but are also able to take your own initiatives. You are organised and incorporate the views of others in your communication and collaboration.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now



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Senior Scientist NMR spectroscopy - consultancy role for 12 months for AstraZeneca

Are you a scientist with expertise in, and passion for, the application of NMR to understand and determine the dynamics and structure of therapeutically relevant target proteins? Would you like to apply your expertise to impact and expand the use of NMR in drug discovery projects whilst being presented with a professional development opportunity within a company that follows science and turns ideas into life changing medicines? Then AstraZeneca has a challenge for you!

AstraZeneca is committed to the development of the next generation of innovative medicines and is focused on expanding the use of small molecules to treat dyslipidaemia and familial hypercholesterolaemia. The company currently exploits new avenues for lowering LDL cholesterol in patients at risk of cardiovascular disease in order to provide additional disease treatment opportunities. To help us with this, we are looking for a scientist with passion, expertise and experience to join our Mechanistic and Structural Biology Department (MSB) as a lab-based Senior Scientist on a one-year contract basis within the Biophysics group in Gothenburg, which is part of the global Discovery Sciences area in AstraZeneca's BioPharmaceuticals organisation.

The MSB department has leading capabilities in biophysics, crystallography, cryo-EM, enzymology and cellular pharmacology. The Biophysics team has specific expertise in molecular biophysics methods, including SPR, NMR, ITC, DSF, HDX-MS, nMS and single molecule approaches. We apply biophysics across a range of different modalities to support drug discovery from target validation to drug candidate.

What you will do:

The role as Senior Research Scientist is a laboratory-based position supporting the structure determination of protein-drug complexes in solution utilising NMR spectroscopy. For this we are seeking a highly skilled and motivated NMR spectroscopist to join our Biophysics team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in pulse sequences for solution-state NMR, along with extensive experience in the assignment and determination of protein structures using NMR techniques. This role is crucial for advancing our research and development projects in dyslipidaemia and familial hypercholesterolaemia.

You will have a high level of control and influence over the project, allowing you to shape its direction and outcomes significantly. Additionally, you will have ample opportunities to learn new technical skills and develop leadership abilities. Our collaborative and innovative work environment enables you to work alongside scientists and postdocs from various disciplines, both within and across the global AstraZeneca community. This role offers a unique opportunity for professional development in an industrial setting, providing you with a valuable experience and additional skills and helping you build a strong foundation for your future endeavours.

You will be responsible for designing and implementing advanced pulse sequences for solution-state NMR, tailored to our specific research needs. You will perform intricate NMR experiments aimed at the assignment and structural determination of proteins, ensuring precise and accurate data collection. Your expertise will be crucial in analysing NMR data, interpreting results, and integrating these findings with other research data to provide comprehensive insights into the drug mechanism of action. You will collaborate with multidisciplinary teams, contributing to the synthesis of NMR findings with the broader research objectives of this project. Additionally, you will stay abreast of the latest advancements in NMR spectroscopy and protein structure determination, continuously applying this knowledge to enhance our research capabilities.

Your findings will not only support the ongoing project but will also constitute an important part of our publication strategy, aiming for high-impact journal publications. You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward.

Finally, to be successful in this role, we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal-oriented and problem-solving attitude.

Why AstraZeneca Gothenburg?

With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, 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.

Does this sound like your next challenge? Apply today! Visa mindre

Consultancy role for AstraZeneca on a 12-month contract.



Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialised separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You'll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.

We are a global, science-led BioPharmaceutical company and our innovative medicines are used by millions of patients worldwide. With our ground-breaking pipeline comes a bright future - a secure job, exciting opportunities, and varied work. You will be valued. Not only for your unique contribution, skills, and background, but because we recognise people are our greatest asset. Here we are dedicated to being a Great Place to Work.

What you will do:

As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries.

In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.

You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.

Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities for the role:

* Provide hands-on separation science support for drug discovery chemistry using state-of-the art chromatographic instrumentation
* Deliver automated analysis and purification of novel compounds using Liquid chromatography-mass spectrometry (LC-MS) and High-performance liquid chromatography (HPLC)
* Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
* Work within the team to suggest process and infrastructure improvements
* Contribute to a vibrant and entrepreneurial organisation focused on innovation & project delivery; collaborating closely with scientists across the discovery organisation

Why AstraZeneca Gothenburg?

With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, 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.

Does this sound like your next challenge? Apply today! Visa mindre

Formulation Scientist/Product Developer - Konsultroll för AstraZeneca
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.

The arena:
We now have the opportunity for one or several consultants to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg. The assignment is on a temporary basis.

Tasks and responsibilities/The role:
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.

The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.

Essential/desirable for the role:
MSc/BSc in chemistry, pharmacy, chemical engineering, food technology or equivalent. Good knowledge in written and spoken Swedish and/or English is necessary as well as laboratory experience including working with computerized systems. If you have experience from working within the pharmaceutical industry, medical tech, or with manufacturing equipment, this will be an advantage. Solid materials/formulation experience is highly meriting.

As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Quality Advisor - AstraZeneca - Gothenburg - 18-month assignment

Quality Advisor

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.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
We have an exciting opportunity for an 18-month temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chains.

This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products

The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, teaming up with the pharmaceutical development functions and be involved in cross-business processes. To build strong relationships with these functions, knowing their business is key, to give support to projects and develop ways of working that builds for success.
The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim of standardising and simplifying our internal processes.

Typical Accountabilities:
- Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
- Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug products
- Providing quality advice and approval of documentation related to equipment, facilities, IT systems and instruments e.g. maintenance, calibration, validation and change control
- Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
- Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Minimum requirements - Education and Experience
-MSc in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
-Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes
-A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous.
-Experience of interacting effectively across interfaces and collaborating internally. Working in a fast-paced environment, meeting deadlines and balance multiple priorities. You are used to team work, networking and an experienced communicator, effectively interacting across interfaces and collaborations.
-Fluent in written and spoken English

As a person, you should have the ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude as well as Excellent team-working and networking skills and encouraging team effectiveness are skills that you possess. We also believe you are a good communicator with experience of interacting effectively across interfaces collaborating internally.

About AstraZeneca Gothenburg Hub, Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centres. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now



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Consultancy role for AstraZeneca - based in Gothenburg - 2-month assignment

Development Quality Consultant, Microsoft 365 (SharePoint/PowerApp) - Process Mapping & Doc System Interface

Description of role
The Development Quality Consultant, Microsoft 365 (SharePoint/PowerApp) - Process Mapping & Doc System Interface will lead the creation of a visually engaging "Quality Management System (QMS) House" to enable visualisation of our business processes and route the user via direct links to filtered views of our Quality Management System (EQV ECMS). The EQV Enterprise Content Management System (EQV ECMS) houses all GxP documentation and is central to our Quality Management System.
The role involves designing a user-friendly SharePoint site that allow users to visually navigate process levels and selecting impacted business areas to find procedural documents relevant to specific areas. This will make up of approximately 600 direct links to filtered views in EQV ECMS to include all available process levels and impacted business areas.
The consultant will ensure the digital interface is intuitive, user-friendly, and visually compelling and will support adoption and roll-out across various business functions by adding relevant information to the page. The page can be built with or without using the Power Apps as part of the solution. But it must be easy to maintain after implementation for updates to links and information for someone with a fundamental understanding of SharePoint.

Accountabilities/Responsibilities

* Architect and implement a visual and digital solution within SharePoint and the Power Platform to streamline document access.
* Create the filtered views in the EQV ECMS and implement to the SharePoint page.
* Ensure the digital interface is intuitive, user-friendly, and visually engaging.
* Collaborate with the Quality Systems team and internal stakeholders to ensure effective linkage to EQV ECMS.
* Design and deliver training and support materials to facilitate system adoption.
* Establish a maintenance plan for the visual QMS House to ensure long-term usability and ease of updates.

Minimum Requirements

* Proven experience with SharePoint and Power Platform design and implementation.
* Familiarity with Quality Management Systems in a pharmaceutical or similarly regulated environment.
* Understanding of document management systems and creating filtered views based on metadata.
* Ability to work independently and manage time effectively to meet project deadlines.
* Strong communication skills for collaborating with cross-functional teams and enabling system adoption.

Education and Experience

* Bachelor's degree in Quality Engineering, Information Technology, Computer Science, or a related field.
* Experience working with PowerBI and PowerApps is highly desirable.
* Previous involvement in projects at the intersection of IT and Quality within a pharmaceutical context is desirable.

Functional & Business knowledge

* Understanding of the importance of GxP documentation and regulatory requirements in the pharmaceutical industry.
* Knowledge of document control practices and the importance of accurate tagging and categorisation.

Skills and Capabilities

* Technical proficiency with SharePoint and the Power Platform, including Power BI and PowerApps.
* Strong analytical and problem-solving skills.
* Excellent interpersonal and change management skills to drive adoption of new systems.
* Ability to create user-friendly and visually appealing digital interfaces that simplify complex processes.
* Commitment to delivering high-quality work within a defined timeline.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Research Scientist position - in vitro cellular profiling
We are looking for a passionate Research Scientist to join our Mechanistic and Structural Biology department within the Discovery Sciences organization in Gothenburg, Sweden. You will apply your proven cell biology expertise to in vitro cellular assays. Routine profiling will be combined with tailored mechanism of action studies in cellular models across a multitude of different drug discovery projects. You will build a detailed understanding of the impact of treatment by multiple drug modalities, including small molecules, PROTACS and therapeutic oligonucleotides.
You will demonstrate a passion for applied science, combined with a strong emphasis on team work. You will join a team whose remit is to support our drug discovery projects globally with early DMPK assessment, SAR profiling and detailed mechanism of action data. We offer a highly rewarding scientific environment with ample learning opportunities.
You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions and make bold decisions.

What you will do:
This is a lab-based role focused on generating routine screening data and bespoke in vitro pharmacology studies in support of drug discovery projects. The work includes independent troubleshooting and timely reporting of data according to agreed timelines. All work is conducted in close dialog with project teams, specifically in support of the Cardiovascular, Renal and Metabolism as well as Respiratory & Immunology disease area organisations locally in Gothenburg.

Essential to the role and desirable skills:
- MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
- Proven track record of cellular biology techniques and pharmacology studies.
- Compound profiling in a screening environment using microtiter plates and automation as well as experience in the design, development and validation of biological test assays for compound profiling.
- Practical knowledge of high-resolution MS for targeted or global proteomics analysis and several technology platforms such as imaging, flow cytometry and LC-MS
- Good knowledge of oral and written English is a requirement

Soft skills:
Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment.
Independent analysis and evaluation of complex data and delivery of data to agreed timelines.
First-rate decision-making skills, coupled with tenacity to see decisions through, even in situations of ambiguity.

Why AstraZeneca in Gothenburg?
You can ask anybody who has ever set foot here - our Gothenburg site has a vibrant culture that pulls you in! It is a mix of both local and international talent. We welcome the contribution of people from all backgrounds, beliefs and walks of life. So, what's next? If this sounds like your next challenge - please apply today! We look forward to your application!

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

This is a consultancy role for AstraZeneca for 12 months.



Supply Chain Manager for Clinical Trial medications

Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca's trials all over the world. Our goal is to never miss a patient.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that helps millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

What you'll do:
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on-time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Your main responsibilities will include:
* Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
* Ensure effective communication with project teams and key partners across a global network.
* Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
* Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
* Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
* Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career. Visa mindre

Your new company

Quality Assurance Advisor 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 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. The arena Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies. The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca.

We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

The role

As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Typical Accountabilities:

* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
* Provide appropriate Quality Assurance input to business improvement projects
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working. Visa mindre

Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing

Hays Life Science is now looking for a new consultant to become an Analytical Chemist at AstraZeneca in Gothenburg, Sweden. This is a consultant assignment for 8 months.

Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing, AstraZeneca Gothenburg

At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients 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.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
We're looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) in Gothenburg.
You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.

Required Qualifications, Skills and Experience:
-University degree (MSc, PhD) in relevant discipline, preferable with industry experience
-Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
-You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams
-Excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues

If you also have experience in one or more of the following areas - great!
-Industry experience of pharmaceutical development including oral solid dosage form development
-Experience of CMC submissions and work according to GMP
-Skilled in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc
-Track record and keen interest of driving development within analytical science including championing new technologies and solutions

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Senior Specialist Programmer, Late-Stage CVRM Biometrics

Hays Life Science is looking for two consultants for a position of Senior Specialist Programmer, Late-Stage CVRM Biometrics at AstraZeneca in Gothenburg, Sweden. This is a consultant assignment for a year with a preferred start on 6th of May.

Are you interested in becoming part of the group of statistical programming at AstraZeneca R&D? Late-stage Cardiovascular, Renal and Metabolism Biometrics is now looking for a Senior Specialist Programmer for a contract assignment with start as soon as possible.

Join a team of statisticians and statistical programmers to provide programming expertise to the design, conduct, reporting, interpretation, documentation, and regulatory submissions of our clinical development programs. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and processes.

Requirements for the role:
* Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering.
* Expertise in drug development and clinical data standards (CDISC)
* Expertise in ADaM (specification writing, programming, define generation and ADRG)
* Expertise in analysis output programming (Tables, Figures etc.)
* Good written and spoken English.

Desirable for the role:
* Expertise in multiple programming software such as R or Python
* Project management experience
* Good collaboration, communication and influencing skills
* Experience from regulatory submissions

Personal Qualities:
* Candidates should possess good social skills, be a strong team player and be able to work effectively in a global organization where teams often are geographically dispersed.
* You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.
* It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them.
* Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development.

Why AstraZeneca?
Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

What's next? If this sounds like your next challenge - welcome to apply! Visa mindre

Hays Life Science is now looking for a new consultant to become a Senior Scientist in Genome Engineering at AstraZeneca in Gothenburg, Sweden. The assignment is to start in the middle of April and will last until the end of January 2025.

Here at AstraZeneca, we are working towards turning novel state-of-art technologies into effective and safe medicines for severe genetic disease. Do you want to be part of this effort? Welcome to join our exciting journey!

We are looking for a new team member to join our Screening and Automation team in Genome Engineering Department. The role is based in Gothenburg, Sweden, where you will join an international team that develops novel genome engineering technologies and applies these technologies for generation of therapeutic agents. We provide a stimulating environment for innovation and translational application of genome engineering tools. We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas.

What you will do:
You will bring your scientific expertise in molecular biology and innovative thinking to drive genome editing approaches that can lead to therapies. You will be a part of cross-functional project teams with various backgrounds and expertise, where you will contribute to development of gene editing strategies.

Accountabilities will include experimental optimization of genome engineering tools to facilitate efficient gene editing, developing relevant assays, analyzing gene editing outcomes, documenting, interpreting, and communicating results to relevant partners. You will collaborate with others to develop streamlined platforms for high-throughput screening and optimization of genome editing components. This is a very exciting role that will give you exceptional professional and technical development opportunities in this state-of-the art scientific discipline.

We also believe that our new colleague is a person who thinks in a creative way and find innovative approaches to scientific problems. You are enthusiastic and curiosity-driven towards finding answers to scientific questions, coming up with solutions to technical problems and learning new skills. You can work in an independent and goal-oriented way, but you also enjoy team work and have the ability to communicate and collaborate in a global setting with cross-functional groups.

Why AstraZeneca?
If you are passionate about translating scientific advances into next generation medicines, AstraZeneca is the right place for you. Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

What's next? If this sounds like your next challenge - welcome to apply! Visa mindre

At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients 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.

Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials and the collection, handling and access to HBS are subject to strict regulations, principles and ethical guidelines.

The HBS Compliance Associate Director is responsible for ensuring the compliant use of samples for research.
They are experienced in the review of informed consent and able to ensure samples are used in accordance with patient wishes, protecting our License to Operate.
They will ensure HBS Compliance procedures are followed with regard to HBS specific policies and standards, and can advise stakeholders on use of samples, including decision making on approval of requests for their use in research.

Typical accountabilities:
Review and advise on use of HBS in accordance with patient consent.
Lead the identification and establishment of effective HBS compliance procedures to support review of samples as part of US inventories.
Manage HBS processes to ensure standards are adhered to and compliance requirements are consistently applied for use of HBS in research for samples in the US for the Amnesty project.
Support the business with compliant use of HBS through expert advice and decision making
Ensure risks arising from HBS due diligence activities for US Inventory are identified and recorded.
Maintain the documentation/SOPs associated with HBS due diligence activities for the US Amnesty project.
Monitor the effectiveness of HBS due diligence processes and identify opportunities for improvement.
Perform HBS due diligence reviews for AZ clinical sample use and re-use requests for HBS in the biobank to support delivery of timely and effective decisions.
Act as subject matter expert, reviewing informed consents and making recommendations on HBS use

Required Skills/ Experience/ Education/ Qualifications:
-Bsc. degree
-Experience in pharmaceuticals, a healthcare related industry or academia/hospital environment related to HBS
-Experience in the review of ICFs regarding use of HBS and knowledge of HBS regulations, laws and standards
-Experience of working with multiple stakeholders while maintaining ethical standards and willingness to challenge inappropriate proposals/actions of senior leaders
-Experience in collection and use of HBS as part of ongoing clinical trials is desirable
-Previous experience as a process owner and process improvement is desirable
-Excellent analytical, written and oral communications skills
-Strong collaborative, partnering, and interpersonal skills
-Strong ability to work independently
-Willingness to take decisions
-Excellent knowledge of English, both written and spoken

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies.
From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre

Quality Assurance Specialist

Quality Assurance Specialist / AstraZeneca / 12 months / Hays Life Science / Göteborg, Sweden



Hays Life Science is now looking for two new consultants to become Quality Assurance Specialists in Göteborg, Sweden.



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 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. The arena Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies. The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca.



We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase. The role As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.



Typical Accountabilities:



* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials

* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities

* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards

* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects

* Provide appropriate Quality Assurance input to business improvement projects

* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working. Visa mindre

Formulation Scientist/Product Developer

Formulation Scientist/Product Developer / AstraZeneca / 10 months / Hays Life Science / Gothenburg, Sweden

Hays Life Science is now looking for a new consultant to become the Formulation Scientist/Product Developer in Gothenburg, Sweden.

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. At AstraZeneca, 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 now have the opportunity for one consultant to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg.



Tasks and responsibilities/The role:

We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.

The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.



Minimum requirements:

* MSc or PhD in chemistry, pharmacy, chemical engineering, food technology or equivalent.
* Good knowledge in written and spoken Swedish and/or English is necessary.
* Laboratory experience including working with computerized systems.
* If you have experience from working within the pharmaceutical industry or with manufacturing equipment, this will be an advantage.



Desirable requirements:

As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.



AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Visa mindre