Lediga jobb som Forskare, farmakologi i Göteborg

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.

About the position
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 product, 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, among others within Continuous manufacture, 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.

Responsibilities
• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform 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 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.

Your profile
Do you have the essential qualifications for these roles?
We are looking for a Scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, team work and delivery focus.
- MSc or BSc in pharmacy/engineering or extensive GMP-manufacturing experience from the pharmaceutical industry
- Excellent collaboration, communication, and planning skills
- Strong sense of responsibility, teamwork and delivery focus
- Strong verbal and documentation skills in English
- Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of GMP is a merit for this role.
- Keen interest to learn and operate complex manufacturing equipment

About the organisation
This position is a consultant assignment at AstraZeneca for 6 months, with a chance of extension. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER Visa mindre

At AstraZeneca, we unlock the power of What Science Can Do. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying, and even curing complex diseases.
KellyOCG, a global talent solutions provider, is seeking an Operational Technologist/Associate Scientist on behalf of our partner, AstraZeneca. This 6-month contract role is based onsite in Gothenburg, Sweden, where you will be fully integrated with the AstraZeneca team, reporting directly to the onsite manager.
Pharmaceutical Sciences at AstraZeneca is responsible 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. Within this function, the manufacturing unit of Early Product Development and Manufacture (EPDM) in Gothenburg is accountable for the production of investigational medicinal products (oral solutions/suspensions, parenteral solutions, capsules, tablets, and inhalers), mainly for clinical Phase I and II studies.
In this position, you will play a crucial role in the production and development of investigational drug products within a GMP-regulated environment, supporting clinical studies and collaborating with AstraZeneca’s experts.
What You Will Do:
Perform hands-on work in AstraZeneca's GMP facilities, contributing to the manufacturing of drug products in development for clinical studies.
Support EPDM Scientists/Senior Scientists and GMP operators with:
Preparation of process rooms before and after clinical manufacturing.
Assembly, disassembly, and cleaning of equipment.
Dispensing of API (Active Pharmaceutical Ingredients) and excipients (inactive pharmaceutical ingredients).
Bulk packing, visual inspection, and metal checking of drug products.
Maintenance of logbooks and adherence to Safety, Health, and Environment (SHE) and GMP standards.
Assist in addressing short-term bottlenecks and supporting manufacturing processes under supervision.

Essential Requirements:
A proactive and detail-oriented mindset, with excellent collaboration, communication, and organizational skills.
An interest in learning and operating complex manufacturing equipment.
Strong verbal and written communication skills in English.

Why Join Us?
This role offers a unique opportunity to work in a dynamic, collaborative environment, contributing to the development of life-changing medicines. You will gain hands-on experience in pharmaceutical development, supported by a team of skilled operators and scientists.
Contract Details:
Duration: 6 months.
Location: Onsite at AstraZeneca, Gothenburg, Sweden.
Application Deadline: January 23rd. Early applications are encouraged as interviews will be conducted on a rolling basis.

If you are driven by curiosity and courage and inspired by the possibility of doing things that have never been done before, this is the place for you. Join KellyOCG and AstraZeneca to make an impact on the future of healthcare! Visa mindre

Are you ready to work in a dynamic and innovative environment where you can make a significant impact on pharmaceutical development? AstraZeneca’s Early Product Development and Manufacture (EPDM) unit in Gothenburg is looking for an enthusiastic Scientist to join their Pharmaceutical Sciences department. In this position, you’ll play a vital role in developing new treatment methods for patients worldwide.

About the role

As a Scientist at AstraZeneca, you will work in a Good Manufacturing Practice (GMP) environment within the EPDM unit. Your primary focus will be on manufacturing investigational drug products for clinical trials. The role includes practical work in GMP facilities, maintaining regulatory compliance, and contributing to process improvement initiatives. You will also have opportunities to deepen your expertise in innovative technologies, such as continuous manufacturing, based on your experience and interests.

Key responsibilities include:

• Manufacturing drug products in accordance with established manufacturing documentation and material handling systems.
• Ensuring timely production in collaboration with EPDM and other stakeholders.
• Monitoring regulatory compliance with GMP requirements and relevant IT systems.
• Supporting documentation processes, such as authoring batch records, SOPs, and investigating deviations.
• Driving process improvements to enhance flexibility, productivity, and value for patients.
• Ensuring adherence to safety, health, environmental (SHE), and GMP standards.

About you

We are looking for a driven, innovative, and detail-oriented individual with a strong passion for pharmaceutical development. You should have experience working in GMP environments and a solid understanding of regulatory requirements in the pharmaceutical industry. To succeed in this role, you need to be solutions-focused, self-reliant, and comfortable working in a dynamic workplace.

Qualifications:

• Academic degree in a relevant field (e.g., chemistry, biotechnology, or pharmacy).
• Experience in GMP manufacturing of pharmaceutical products.
• Strong proficiency in English, both written and verbal.
• Experience from working in a supply chain organisation is a merit for this role.

As One of Us

As an employed staffing consultant at Lernia, you will always receive a competitive salary, vacation benefits, pension contributions, insurance coverage, and be part of our collective agreement. We care about your well-being, which is why we offer all our consultants wellness allowances and access to occupational health services. During your employment, you will have a dedicated consultant manager responsible for your assignment, ensuring you thrive at your workplace while supporting and developing you in your professional role.

About Lernia

Lernia is one of Sweden's leading staffing and recruitment companies, with a presence across the country. Through our extensive network, we offer exciting jobs with attractive employers and brands, helping you develop your skills and career, both in the short and long term.

How to Apply

To apply for this position, click on the "Apply" link above and fill out the form. For any questions or inquiries, please contact recruiter Oscar Sahlin at [email protected].

We conduct interviews on an ongoing basis, so please submit your application as soon as possible! Visa mindre

Vill du bli en del av AstraZeneca i sommar? Vi på KellyOCG i nära samarbete med AstraZeneca söker nu engagerade medarbetare för varierande uppdrag under juni–augusti 2025 med placering i Göteborg eller Södertälje.
Denna annons är främst en spontanansökan/intresseanmälan och riktar sig mot dig som tidigt vill uttrycka ditt intresse för möjligheten att arbetat på AstraZeneca.
Mer information och specifika arbetsbeskrivningar kommer dyka upp i början av 2025 men vi vet redan nu inom vilka områden vi söker nya medarbetare (Se nedan).


Exempel på områden där vi erbjuder sommarjobb:
Administration och generalistroller (Södertälje & Göteborg)
IT (Göteborg)
Life Science (Södertälje & Göteborg)
Produktion och tillverkning (Södertälje)



Detta är en unik möjlighet för dig som vill utvecklas och ta del av den kunskap som finns inom AstraZenecas olika arbetsområden.


Skicka in ditt CV redan idag och ta chansen att utvecklas i en innovativ och global miljö!
Varmt välkommen med din ansökan! Visa mindre

About the position
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.

Responsibilities
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 to execute 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, emphasizing a “can do” attitude and ensuring high standards of quality in all outputs.

Other key responsibilities in this position:
• Identify opportunities for and drives the enhancement of existing processes and procedural documents
• Using understanding of regulatory processes and regulations to provide support to 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

Your profile
Essential for the role:
• A science/pharmacy/nursing degree, with relevant experience (pharmaceutical, regulatory, safety)
• Exceptional attention to detail and accuracy
• Excellent written and verbal communication skills in English
• Knowledge of the drug development process and sufficient knowledge to understand aspects of Regulatory
• Experience in working cross-functionally
• Proven ability to work across cultures

Desirable for the role:
• MSC/PhD in scientific discipline
• Knowledge of regulatory expectations and regulations
• Knowledge of existing AstraZeneca organisation
• Experience of working in a global organisation, preferably within the pharmaceuticals industry, and of the drug development life cycle

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg from January 2025 until end of August 2025. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

For our close partner AstraZeneca, KellyOCG is seeking a Sr Scientist - Solid State for a contract (6 months initially with high possibility of 6 additional months) with the added possibility of contract extension and further collaboration opportunities. You will work entirely onsite at AstraZeneca in Gothenburg / Mölndal, becoming an integral part of their team and reporting directly to their manager.
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”.
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 into phase II. 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 substance and product. 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 characterization data in our state of the art laboratory using techniques like TGA, DSC, XRPD and DVS.
• Responsible for ensuring suitable physical form screening, characterization, 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
Requirements
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.
Essential for the role:
• Master/Bachelor graduate with relevant experience in solid-state chemistry, physical chemistry, or related disciplines.
• Experience in screening and characterization of solids, analytical methodology, and laboratory-based work.
• Experience from conducting solid-state characterization using techniques like TGA, DSC, XRPD, or DVS.
Desirable for the role:
• Interest in lab automation, simulation, or prediction is advantageous.
• Understanding of how physicochemical and solid-state properties affect drug product development.
Soft skills:
• Creativity, innovation, and problem-solving skills.
• Ability to assess, review, and report data, and present findings in multi-disciplinary teams.
• Flexibility, adaptability, and strong communication, teamwork, and leadership skills.


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 than 50 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.
The final application date is November 27th, but we encourage early applications as positions may be filled before the deadline. We will review applications and conduct interviews on a rolling basis.
Does this sound like your next challenge? Apply today! Visa mindre

About the position
We are now looking to recruit an In Vivo Scientist with excellent laboratory skills and a drive for innovation to join the Bioscience in vivo department within the Early Respiratory and Immunology (eR&I) R&D unit located in Gothenburg, Sweden.

Respiratory and immunology are two of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify, and ultimately cure respiratory disease with an emphasis on four respiratory diseases with significant unmet medical need: asthma, COPD, Idiopathic Pulmonary Fibrosis (IPF) and Chronic Cough. In addition, we also focus on immunology-driven disease areas including rheumatology, dermatology, gastrointestinal and inflammatory diseases driven by eosinophilic immune dysfunction.

The successful candidate will join a highly motivated team that works closely together with other departments focusing on target identification, drug formulation, translational science, in vitro assay development and drug metabolism/pharmacokinetics to support discovery projects and to drive exciting new research. Are you ready to join us?

Responsibilities
As a vital member of our in vivo team, you will contribute to progress our drug discovery projects. Your role will be mainly lab-based in which you will be actively involved and responsible to coordinate, perform and analyze in vivo studies. While we expect you to be independent, we are also looking for someone that thrives in a team setting and contributes to the success of others.

Your profile
• B.Sc. or M.Sc. degree in relevant subjects or equivalent level of understanding developed through experience in drug discovery or early development.
• Excellent technical and experimental In vivo experience and skills, including rodent handling, drug administration and collection of biological samples. Ability to coordinate and perform respiratory disease and mechanistic models.
• Valid certificates to work with live animals in Sweden.
? Excellent written and oral communication skills in English.
? Maintain the highest standards of animal welfare and ethical compliance and ensure integrity of generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R’s (reduction, refinement, and replacement) across the full range of studies.
? Good generic computer proficiency including Microsoft Office.

About the organisation
This is a consultant assignment for 12 months, starting in January 2025 at AstraZeneca in Göteborg. During this time you will be hired by QRIOS.
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

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 characterization 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.

Your profile
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 utilize scientific and innovative thinking.
• Genuine interest in experimental work and hands-on problem solving.
• Great communication skills in English, both orally and in writing.

About the organisation
This is a consultant assignment for 1 year, startin 2025-01-08 at AstraZeneca in Göteborg. During this time you will be hired by QRIOS.
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

If you’re ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And you’ll be developing yourself in a global environment with an inspirational culture, with lots of opportunities. All the while building a successful career, with real purpose.
We are looking for a Senior Scientist – Tissue & Wound Science
to secure research and early development within the area of tissue and wound science research.
This is a fantastic opportunity to be part of our great team within the Science & Technology department within our R&D Wound Care organization. You will interactwith our R&D laboratories, product development function and regulatory department to mention a few.
In this position you’ll be stationed at our new headquarters at GoCo Health Innovation City, a world-class innovation cluster for health!

About the job
As a Senior Scientist in the Tissue & Wound Science team you will be a key person to lead the exploration and development of new and/or improved active/healing & antimicrobial materials and concepts to meet customer needs.
You’ll provide scientific preclinical understanding and evidence to drive and support early development projects and create and maintain a scientific network to be in the scientific forefront in wound care.

These are the main accountabilities for this position
In this position you will continuously search for and propose new conceptual product solutions to meet customer needs.
You will lead or participate in identified applied research projects and provide results within the tissue and wound biology as well as microbiology areas as defined by the project plan to reach the project objectives to develop new and/or improved concepts and products. Initiate contacts and co-operation with external institutes, universities, suppliers etc. to find new and improved solutions to customer needs.
You will continuously acquire knowledge in the area of tissue & wound biology in the scientific literature on substances and materials as well as competitor products to improve solutions to meet customer needs, to identify new trends and opportunities and to match with business requirements.
In this role it will be of importance to build an international external network and represent Mölnlycke and conduct research collaborations with academia and industry.
You will lead development and/or search for new in vitro and in vivo models to measure or demonstrate product and material performance.

What you'll need
Academic background in engineering or life science (PhD, Master Degree) or corresponding experience.
Minimum of 8 years experience within Medical device/Pharma or similar fields
Knowledge in tissue/wound biology & microbiology
Experience in biomarker research linked to applications of bioinformatics and data analysis
Project management experience is considered a merit
Scientific and business mindset with experience of preclinical method development and implementation
Experience in external collaborations
Good communication skills and happy to work in a dynamic team
Performance driven and customer focused



What you’ll get
Wellness benefits
Flexible working hours
Great colleagues in a global company
An open, friendly and fair working atmosphere
Competitive compensation package including company pension plan, bonus, company health care



Our approach to diversity and inclusion
At Mölnlycke diversity is not just a vision, but our strength. We are dedicated to fostering an inclusive workplace that values and celebrates the power of diversity. At the heart of our commitment is the belief that diversity fuels innovation, creativity and problem-solving. We invite you to be a part of a team where authenticity is embraced, and every employee, regardless of background or any other traits, experiences a true sense of belonging. Your attitude, drive, enthusiasm, and eagerness to learn are just as important to us as the requirements for the role.

About Mölnlycke
Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes. Our business is organized in the four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics, where customer centricity, sustainability and digitalisation are at the heart of everything we do.
Mölnlycke employs around 8,700 people. The company headquarters are in Gothenburg, Sweden and we operate in more than 100 countries worldwide. Mölnlycke is a founding partner of GoCo Health Innovation City, a world-class innovation cluster for health, and in early 2025 our headquarters will move there. Since 2007, the company has been part of Investor AB, an engaged owner of high-quality, global companies which was founded by the Wallenberg family in 1916.
For more information, please visit www.molnlycke.com and www.molnlycke.com/careers
If this sounds like you and you feel you have what it takes to succeed in this role, we want to hear from you as soon as possible. Visa mindre

AstraZeneca is offering year-long, monthly salaried student work placement opportunities in Pharma R&D, Bioscience and Data Science & AI. (1 års betald praktikplats)
About AstraZeneca
AstraZeneca is a global, science-led biopharmaceutical business and its innovative medicines are used by millions of patients worldwide. AstraZeneca has long been an advocate of student work placement training and considers it our responsibility to help promising scientists grow into the researchers of the future.
12-Month Student Work Placement Opportunities with AstraZeneca
Don’t miss the opportunity to explore your interests, gain work experience and build a professional network. To support you in this journey, AstraZeneca Sweden has partnered with consultancy KellyOCG, who aside from helping with the Work Placements also manages the summer jobs and consultant contracts giving you even better opportunities for continued futured possibilities!
The Work Placement Opportunities
Commencing September 2025, you will be provided with the opportunity to undertake a 12-month placement in Gothenburg that will introduce you to the world of innovative drug discovery pushing the boundaries of science to deliver life-changing medicines.
We offer Work placements in these areas:
Biopharmaceuticals R/D
Translational Genomics
Assays & Profiling
Chronic Obstructive Pulmonary Disease (COPD) / Idiopathic Pulmonary Fibrosis (IPF)

Chemistry
Early Chemical Development
Advanced Drug Delivery
Early Product Development & Manufacturing (EPDM)

Data Science and AI
Molecular AI
Data Science & Advanced Analytics
Centre for AI

Early Respirator & Immunology-In Vivo
Image Analysis and Platform
Protein Structure & Biophysics
As well as developing the skills, knowledge and network that will set you up for success, you will be among curious, passionate and open-minded people eager to learn, follow the science, helping you grow as professionals in a truly collaborative and global team.
Explore our open opportunities to unlock your potential at AstraZeneca!
Applications are now open until January 2025, with interviews to take place in March 2025. Start date 1st September 2025. Applications must be submitted in English.
This internship is a collaboration between AstraZeneca and Kelly Services. The employment relationship is with Kelly Services partner, Poolia AB.
Here you will find the different Work Placements and how to apply to them: https://toptalents.com/AstrazenecaSe-Earlytalent/search Visa mindre

Are you a scientist with expertise in Surface Plasmon Resonance (SPR) and a passion for applying biophysical tools to advance drug discovery? Do you want to expand the impact of SPR and related techniques in transformative research projects, while growing your career at a company dedicated to developing life-changing treatments? AstraZeneca has an exciting opportunity for you!

Brief information about the assignment

Location: Gothenburg (Mölndal)
Job Type: Consultancy assignment
Assignment Duration: 2025-01-15 to 2026-01-14, with a strong possibility of extension

About the Role

As a Senior Scientist, your main focus will be on characterizing molecular interactions using Surface Plasmon Resonance (SPR) and other cutting-edge biophysical techniques. In this one-year contract position, you will design and implement advanced SPR assays, optimize methods, and conduct screening activities to support drug discovery efforts across multiple therapeutic areas.

In this role, you will:

• Lead the design, optimization, and execution of SPR assays for complex research projects.
• Conduct in-depth experiments to understand binding kinetics, affinity, and thermodynamics, ensuring accurate data collection and analysis.
• Integrate SPR data with broader research findings to provide a comprehensive understanding of drug mechanisms.
• Collaborate with multidisciplinary teams to ensure that SPR and biophysical findings contribute meaningfully to research outcomes.
• Stay up-to-date with the latest advancements in SPR and related biophysical technologies.

This position offers you the opportunity to significantly shape project directions and outcomes, while also learning new techniques and developing leadership skills in a collaborative environment. AstraZeneca encourages innovation and professional development, providing an ideal setting for scientists looking to make a meaningful impact in drug discovery.

Requirements

• Ph.D. or equivalent in Chemistry, Biochemistry, or a related field with a focus on biophysical techniques to characterize molecular interactions, preferably SPR (or something similar system)
• Extensive experience with SPR and other biophysical techniques such as NMR, ITC, DSF, HDX-MS, and single molecule methods.
• Proficiency with surface-based biosensor platforms (e.g., Biacore, Nicoya, Octet, WAVEsystem) including assay development and optimization.
• Expertise in developing, troubleshooting, and optimizing biosensor assays for high-throughput screening and kinetic data analysis, with proficiency in data analysis software (e.g., Biacore Insight, WAVEcontrol) and protein sample preparation to ensure high-quality samples for biophysical studies.
• Strong theoretical and practical knowledge in protein-ligand interactions.
• Proven ability to work both independently and as part of a team, with excellent communication skills.
• A goal-oriented, problem-solving attitude, with a passion for contributing to impactful scientific discoveries.

Why Join AstraZeneca?

At AstraZeneca, they seize opportunities to drive change and make a real impact in healthcare. By joining them, you will contribute to life-changing medicines and pioneering research, while working in a stimulating and innovative environment. Take this chance to be part of a team that’s finding new ways to transform ideas into reality.

How to Apply

To apply for this position, click on "Apply" above, fill out the form and attach your CV. A cover letter is optional. If you have any questions or concerns, please contact recruiter Oscar Sahlin at 072-204 84 03.

Lernia – The Path Forward

Lernia develops the workforce of the future. We do this by educating, matching, staffing, and recruiting. Quickly and hassle-free, we address the needs of the labor market so that individuals and companies can reach their full potential. This has been our mission for over 100 years. In 2023, Lernia had a turnover of SEK 3.5 billion and operates across the country, from south to north, in around 100 locations. We educated and coached 18,400 people and provided 10,900 staffing consultants. Through our services, 12,000 individuals were given opportunities for new jobs. Visa mindre

About the position
Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

The DPD Operator role will be an operational role within Distribution or Material Management two of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in a environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:

- Distribution experience from a complex supply chain organization
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Responsibilities
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused operational within Distribution or Material Management. As a DPD operator you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and manage deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.

Responsibilities example:
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.


Your profile
Essential requirements and skills
• BSc/MSc in chemistry/pharmacy/engineering/logistics or equivalent experience. Preferably 2 years experience within pharmaceutical development.
• Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally.
• Good written and verbal English communication and understanding.

Beneficial requirements and skills:
• Understanding of principles, applications and management of SHE and GMP in an R&D environment.
• Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization.

Soft skills:
• Curious and innovative mindset with problem solving ability - resolve issues with minimal guidance

About the organisation
This is a consultant assigment until end of September 2025 at AstraZeneca in Gothenburg. During this time you will be hired by QRIOS.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

About the position
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 next generation 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.

Responsibilities
The role of Senior Scientist is a laboratory-based position supporting the characterization 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 optimization, 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 analyzing 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.

Your profile
• Ph.D. or equivalent in Chemistry, Biochemistry, or a related field with a focus on biophysical techniques to characterize molecular interactions, preferably SPR (or something similar system)

• Proficiency with surface-based biosensor platforms (e.g., Biacore, Nicoya, Octet, WAVEsystem) including assay development and optimization.

• Expertise in developing, troubleshooting, and optimizing biosensor assays for high-throughput screening and kinetic data analysis, with proficiency in data analysis software (e.g., Biacore Insight, WAVEcontrol) and protein sample preparation to ensure high-quality samples for biophysical studies.

• Familiarity with complementary biophysical methods such as ITC, MST or DSF as well as protein expression, purification, and characterization techniques to ensure optimal sample quality for biophysical assays.

• Proven reputation gained through an excellent track record of publications and/or conference presentations.

Desirable for the role:

Worked in drug discovery environment.


About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

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 or Cambridge, UK.
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.

About the position
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 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 optimize 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 translates this into meaningful Procurement projects
Builds strong relationship 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

Your profile
Essentials for the role
Degree level qualification or relevant experience
Thorough knowledge of 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

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for 1 year.
During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

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

Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 56 000 studenter och 6 600 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.Vid Institutionen för neurovetenskap och fysiologi vid Sahlgrenska akademin bedrivs omfattande forskning och undervisning över stora kunskapsområden - från molekyl till människa. Verksamheten utgörs av fem sektioner; farmakologi, fysiologi, hälsa och rehabilitering, klinisk neurovetenskap samt psykiatri och neurokemi.

Institutionen för neurovetenskap och fysiologi, söker nu en forskare i farmakologi, i synnerhet inom autonoma nervsystemets farmakologi, med placering vid Sektionen för farmakologi. Anställningen berör forskning inom ämnesområdet, men även undervisning och viss administration kan ingå.

Arbetsuppgifter

Arbetsuppgifterna innefattar forskning inom neurofarmakologi med särskild inriktning mot autonoma nervsystemets farmakologi och sjukdomar. I arbetsuppgifterna ingår undervisning i farmakologi. Även handledning av forskarstuderande kan ingå.

Kvalifikationer

Behörig att anställas som forskare är den som innehar doktorsexamen i för arbetsuppgifterna relevant ämnesområde. Arbetet kräver hög kompetens och lång erfarenhet inom det aktuella området samt inom farmakologi som helhet. Omfattande undervisningserfarenhet är ett krav. Administrativ erfarenhet är meriterande för tjänsten. Vi lägger stor vikt vid personlig lämplighet.

Anställning

Anställningen är en tillsvidareanställning, 10% av heltid, med placering tills vidare vid Institutionen för neurovetenskap och fysiologi. Tillträde: snarast eller enligt överenskommelse. Provanställning kan komma att tillämpas. 

Kontaktuppgifter för anställningen

Har du frågor om anställningen är du välkommen att kontakta professor/sektionschef Michael Winder, tfn: +46 31 786 34 77, epost: [email protected]

Ansökningshandlingar skickas inte till kontaktpersonen.  

Fackliga organisationer

Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande

Ansökan

Du söker anställningen via Göteborgs universitets rekryteringsportal genom att registrera din ansökan elektroniskt via hemsidan: https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.

Intyg om doktorsexamen bifogas med ansökan.

Ansökan ska vara inkommen senast: 2024-09-27.

Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten.

Universitetet tillämpar individuell lönesättning.

Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut.

Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser. Visa mindre

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 and an eye for details 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.

About the position
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 product
Providing quality advice and approval of documentation related to equipments, 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

Responsibilities
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.

Your profile
Requirements:
• Degree in pharmacy or engineering (specializing in Pharmaceuticals)
• 2-3 years’ experience of working within a pharmaceutical GMP environment.
• 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.
• Experience preferably within a pharmaceutical manufacturing organization is desirable
• Understanding of Project Management processes is desirable
• Fluent in written and spoken English.

Softskills/personal skills:

• Good team working 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.

About the organisation
This is a consultant assignement for 12 months at AstraZeneca Göteborg. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

Research Scientist Biosamples, Biobank Scientist to AstraZeneca in Gothenburg!

Are you looking for an exciting challenge in the field of bioscience? We are currently seeking a Biobank Scientist to join the AZ Gothenburg Biobank team, part of the global Precision Medicine and Biosamples organization. In this role, you will have the opportunity to work in a dynamic and collaborative environment, where you´ll provide essential support to drug discovery projects. You´ll be part of a team that shares collective responsibility for delivering high-impact results. Ready to make a difference? This could be the perfect role for you!

Purpose, Offer and Benefits

This is a 1-year consulting assignment starting in September. During the assignment period, you will be employed by TNG.

 AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. However, as a company we are more than one of the world´s leading pharmaceutical companies, we are proud to have a unique workplace culture that inspires innovation and collaboration. AstraZeneca employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Your Responsibilities

The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining high quality handling and storage of HBS and support projects with requested samples in a timely manner.

As a Biobank Research Scientist you will be expected to:

• Work as part of the team rotating between the following typical tasks
• Receive and register incoming HBS
• Process requests for HBS to customers, including using automated liquid handler
• Manage customer orders using specialized informatics systems as well as databases
• Respond to customer queries via mail or telephone
• Partner with Biobank groups globally as well as internal and external customers
• Work closely with other groups in the organization
• Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
• Identify initiatives to improve efficiency or quality.

The Bigger Picture

Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within AZ globally to provide efficient support across AZ and our partner organisations.

The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting-edge facility.

Our Expectations

Essential for the role:

• University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
• Previous knowledge and experience (1 year) of biobanking is highly desirable.
• Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
• Experience of automated liquid handling is advantageous.
• Good analytical and problem-solving skills involving large and complex datasets is desirable.
• Excellent English, both spoken and written

Soft skills:

• Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process.
• Knowledge of the regulatory framework of biological samples.
• Interest in logistics and developing processes through customer interactions and technology awareness.
• Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem
• Thrive on working in a committed team and gain satisfaction from the overall performance of the group

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 56 000 studenter och 6 600 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.Institutionen för kliniska vetenskaper, avdelningen för kirurgi, vid Sahlgrenska akademin söker en postdoktor i cancerforskning med inriktning på neurobiologi samt immunologi. Tjänsten tillsätts via finansiering av Wallenberg Centre for Molecular and Translational Medicine och är placerad på Sahlgrenska Centrum för Cancerforskning. Forskargruppen har ett tydligt mål att generera nya måltavlor för cancerbehandling samt att överföra kunskap från grundforskning så att denna kan omsättas till innovativa kliniska prövningar med nya behandlingsprinciper mot lungcancer och malignt melanom.

Tjänsten är placerad Volkan Sayins forskargrupp som positionerar sig i korsningen mellan behandlingsmetoder för lungcancer samt cancerämnesomsättning och redoxbiologi. Vi bygger en plattform för precisionsmedicin, där vi kombinerar de senaste teknologierna inom lungcancerforskning och metabolomik för att etablera en omfattande lungcancergrupp på Sahlgrenska Center for Cancer Research

Ämne 
Cancerforskning med inriktning på neurobiologi samt immunologi

Ämnesbeskrivning 
Syfte med det här projektet är att Identifiera terapeutiska mål för behandling av hjärnmetastaser hos patienter med lungcancer. De flesta dödsfallen hos lungcancerpatienter beror på lungcancermetastaser, där hjärnan är det vanligaste målorganet. Hjärnmetastaser inträffar i cirka hälften av alla fall när sjukdomen fortskrider, och upptäcks hos 21% av patienterna med lungcancer vid första diagnosen. Vi har tagit fram en djurmodell för att undersöka lungcancer-relaterad hjärnmetastas och i det föreslagna projektet ämnar vi undersöka vilken roll membranbundna protein har i lungcancercellers förmåga att ta sig över blodhjärnbarriären och därmed metastaser till hjärnan. Vi ämnar utföra det dels genom så kallad CRISPR/CAS9- screening där vi sänker uttrycket för vissa utvalda membranbundna protein och därmed kan vi undersöka vad de har för betydelse för hjärnmetastasering av lungcancer. Vid positivt utfall ämnar vi syntetisera nya molekyler som vi kan använda för att gå in och döda cancerceller eller möjliggöra att andra läkemedel kan gå in och döda cancerceller. Idag finns det ingen effektiv behandling för hjärnmetastas så om vi skulle finna ett lovande målprotein att påverka så skulle det kunna vara revolutionerande för cancervården. 

Arbetsuppgifter 
I arbetsuppgifterna som postdoktor ingår främst att bedriva forskning inom forskningsområdet. Du kommer att delta i ett forskningsprojekt som fokuserar på att använda nya djurmodeller för att identifiera styrande mekanismer vid hjärnmetastas från lungcancer och utveckla nya behandlingar mot lungcancerrelaterad hjärnmetastas. I arbetsuppgifterna ingår även en stor del laborativt arbete och problemlösning. Arbetsuppgifterna utförs självständigt, men i nära samarbete med både nationella och internationella kollegor. Det förväntas även att du finner och skapar nya relevanta samarbeten. I arbetsuppgifterna ingår även undervisning och handledning av doktorander och studenter på labbet. 

Behörighet 
Behörig att anställas som postdoktor är den som har avlagt doktorsexamen, konstnärlig doktorsexamen eller som har en utländsk examen som bedöms motsvara doktorsexamen. Detta behörighetskrav ska vara uppfyllt senast vid tidpunkten då anställningsbeslutet fattas.

I första hand bör den komma i fråga som har avlagt examen högst tre år före ansökningstidens utgång. Även den som avlagt examen tidigare bör komma i fråga i första hand, om det finns särskilda skäl. Med särskilda skäl avses ledighet på grund av sjukdom, föräldraledighet, förtroendeuppdrag inom fackliga organisationer, tjänstgöring inom totalförsvaret, eller andra liknande omständigheter samt klinisk tjänstgöring eller för ämnesområdet relevant tjänstgöring/uppdrag.  

Anställning 
Anställningen är tidsbegränsad 24 månader på heltid med placering tills vidare vid institutionen för kliniska vetenskaper, avdelningen för kirurgi. Tillträde snarast.  

Ansökan 
Observera att detta är en förkortad version av ledigkungörelsen. För fullständig information om tjänsten, behörighet, bedömningsgrunder, ansökan samt kontaktuppgifter och fackliga organisationer se annonsen på https://www.gu.se/jobba-hos-oss/lediga-anstallningar

 

Ansökan ska vara inkommen senast: 2024-09-12

Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten.

Universitetet tillämpar individuell lönesättning.

Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut.

Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser. Visa mindre

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!
As our new Senior Research Scientist, you will be a part of the Therapeutic Editing team in the Department of Genome Engineering. 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, to turn them into effective and safe medicines.
We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas. We expand the limits of scientific research to better understand diseases and to discover new life-changing treatments for them.


What you will do:
You will bring your expertise in molecular biology or screening sciences to develop novel genome editing approaches that can potentially lead to therapies. You will be a key member in cross-functional therapeutic editing project teams with various backgrounds and expertise, where you will be responsible from establishing screening capabilities and running the screens for therapeutic editing projects.
Accountabilities will include screening and optimization of genome engineering technologies to facilitate effective gene editing in target cell & tissue types, analyzing gene editing outcomes, documenting, interpreting, and communicating results to appropriate partners. You will collaborate with other functions to develop and test novel CRISPR delivery strategies – and to develop high throughput next generation sequencing approaches to analyze gene editing outcomes.
Requirements
• PhD degree?in molecular/cell biology, genetics, screening sciences or relevant areas
• Molecular or cell biology background and relevant hands-on skills
• Expertise in DNA damage and repair
• Expertise in cellular assays, such as genetic manipulation and evaluating genetic & functional outcomes using state-of-art tools including next generation sequencing, qPCR/RNA-seq etc.
Desirable for the role:
• Experience with cell-based high throughput screening methodologies
• Experience in advanced cellular models such as iPS cells and differentiation
• Solid understanding of genome engineering
• Experience in flow cytometry/FACS
We also believe that our new colleague is a person who thinks outside the box and find innovative approaches to scientific problems. You hold enthusiasm and curiosity towards scientific questions 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 - collaborate in a global setting with cross-functional groups.


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.


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

About the position
Inhalation Product Development (IPD) at AstraZeneca is a multinational organization that combines decades of experience in inhalation technology whether it is nebulization, 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 characterization 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 characterization of inhaled products.

Responsibilities
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, utilizing both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.

Your profile
Essential 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 leaning analytical techniques used for inhaled products.
• Excellent communication skills in English, both oral and written.
• Understanding the principles and applications of GMP.

Desirable for the role:
• Experience in aerosol characterization 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.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg until 2025-03-31. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

As our new Senior Research Scientist, you will be a part of the Therapeutic Editing team in the Department of Genome Engineering. 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, to turn them into effective and safe medicines.

We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas. We expand the limits of scientific research to better understand diseases and to discover new life-changing treatments for them.

Responsibilities
You will bring your expertise in molecular biology or screening sciences to develop novel genome editing approaches that can potentially lead to therapies. You will be a key member in cross-functional therapeutic editing project teams with various backgrounds and expertise, where you will be responsible from establishing screening capabilities and running the screens for therapeutic editing projects.

Accountabilities will include screening and optimization of genome engineering technologies to facilitate effective gene editing in target cell & tissue types, analyzing gene editing outcomes, documenting, interpreting, and communicating results to appropriate partners. You will collaborate with other functions to develop and test novel CRISPR delivery strategies – and to develop high throughput next generation sequencing approaches to analyze gene editing outcomes.

Your profile
Essential for the role:

• PhD degree?in molecular/cell biology, genetics, screening sciences or relevant areas
• Molecular or cell biology background and relevant hands-on skills
• Expertise in DNA damage and repair
• Expertise in cellular assays, such as genetic manipulation and evaluating genetic & functional outcomes using state-of-art tools including next generation sequencing, qPCR/RNA-seq etc.

Desirable for the role:

• Experience with cell-based high throughput screening methodologies
• Experience in advanced cellular models such as iPS cells and differentiation
• Solid understanding of genome engineering
• Experience in flow cytometry/FACS

About the organisation
This is a consultant assignement for 12 months at AstraZeneca Göteborg starting in November. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

Do you have organic synthesis expertise? Are you interested in becoming part of an impactful team passioned for science and technology, and focussed on chemistry automation to accelerate drug discovery? Would you like to become part of a company where we are committed to lifelong learning, growth, and development? This might be your next challenge!

We are looking for an Organic Chemist who will play an important part in our interdisciplinary team, implementing state-of-the-art chemistry automation technologies for the high-throughput synthesis of new molecules for projects.

About the position
By using chemistry automation technologies, you will contribute to the optimisation and synthesis of libraries of screening compounds (including traditional small molecules and small molecules degraders) on nanomol and micromol scale to progress projects. You will collaborate with experts in a variety of disciplines, including medicinal chemistry and artificial intelligence, to maximise the impact of our capabilities. You will contribute to the evaluation and development of automation-friendly synthetic methods to access optimal synthetic pathways for the synthesis of desired libraries and make a significant contribution to the team delivery.
You will have access to the best internal and external science and enhance business reputation internally and externally through peer-reviewed publications and oral/poster presentations.

Responsibilities
By using chemistry automation technologies, you will contribute to the optimisation and synthesis of libraries of screening compounds (including traditional small molecules and small molecules degraders) on nanomol and micromol scale to progress projects. You will collaborate with experts in a variety of disciplines, including medicinal chemistry and artificial intelligence, to maximise the impact of our capabilities. You will contribute to the evaluation and development of automation-friendly synthetic methods to access optimal synthetic pathways for the synthesis of desired libraries and make a significant contribution to the team delivery.
You will have access to the best internal and external science and enhance business reputation internally and externally through peer-reviewed publications and oral/poster presentations.

Your profile
You’re a chemist with a track record of applying innovative chemistry solutions, with resulting impact on project delivery. You also have:
• Ph.D. in organic chemistry, or a Master degree in chemistry with minimum 5 years’ experience in synthetic organic chemistry
• Experience in planning and executing chemistry experiments in parallel and adapting existing protocols to new applications
• Expertise in organic synthesis, retrosynthesis, compound route design, purification, and analytical chemistry
Experience in chemistry automation and plate chemistry would be desirable

The successful candidate should encourage innovation and be motivated to work effectively in team having strong communication and collaboration skills. The ideal candidate should demonstrate ability to work across scientific fields, possess a curious mind and a long-term commitment to advancing chemistry automation as an innovative tool in drug discovery.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg during the autumn 2024.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

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 the science and turns ideas into life changing medicines? Then AstraZeneca has a challenge for you!

About the position
AstraZeneca is committed to the development of next generation innovative medicines and is focused on expanding the use of small molecules to treat dyslipidaemia and familial hypercholesterolemia. 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.

Responsibilities
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 analyzing 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 endeavors 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.

Your profile
• Ph.D. or equivalent in Chemistry, Biochemistry, or a related field with a focus on NMR spectroscopy.
• Proven experience in pulse sequence development and application for solution-state NMR.
• Demonstrated expertise in the assignment and determination of protein structures using NMR.
• Proficient in NMR data analysis software and tools and demonstrated ability to communicate data interpretation clearly.
• Familiarity in the general application of biophysical methods for the study of molecular interactions.
• Proven reputation gained through an excellent track record of publications and/or conference presentations.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

We are developing state-of-the-art technologies and models to advance gene and cell therapy approaches. AstraZeneca’s Genome Editing Team in Gothenburg, Sweden, is now looking for a passionate Scientist to innovate in the field of Therapeutic Genome Editing. If you are looking for a fast-paced environment where your scientific insights can translate into meaningful impacts on patient lives, this is the position for you!?

About the position
As a Scientist in the Genome Editing Team, you will join an international group of energetic researchers of various backgrounds who are excited about science and challenge its dogmas. We create a supportive and inclusive environment, and a fun atmosphere for everyone independent of their preferences, experiences and beliefs. Our work focuses on basic yet translational research that is designed to reach the clinics. Especially, we are passionate about modifying genomes at will for therapeutic purposes.

Responsibilities
Our successful candidate needs the ability to communicate, interact and collaborate with other team members, as well as across our AZ global functions and fields. Alongside this, our ideal candidate enjoys working in an innovative, proactive, forward-thinking, project-focused and goal-oriented way and shares our excitement about the latest gene-editing techniques.

Your profile
Essential requirements:
-A relevant science degree (MSc or BSc) ( 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 benificial.
- 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 organized and incorporate the views of others in your communication and collaboration.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

We are seeking a motivated Discovery Safety Scientist/ Senior Scientist In Vitro Biology to AstraZeneca in Gothenburg

Are you a motivated cell biologist with experience of in vitro work in molecular biology, omics and oligonucleotides? Do you enjoy working hands-on in the lab with a great group of colleagues by your side? If yes, this might be the next position for you!We are looking for a highly engaged and enthusiastic cell biologist to join as a Discovery Safety Scientist and complement us in our In Vitro Safety group at AstraZeneca in Gothenburg.

Purpose, Offer and Benefits

This is a one year consulting assignment starting end of July 2024 and will continue until end of July 2025. You will be employed by TNG during the assignment period.

Working in an industry-leading in vitro safety lab, you will collaborate with internal research teams to identify potential off-target risks for siRNA/antisense oligonucleotide (ASO) projects. This involves developing in vitro assays to investigate these off-target effects in various mammalian cell types through gene expression analysis. Additionally, you will summarize safety-related literature on the modulation of off-target genes to aid in decision-making and support the development of safer oligonucleotide-based drugs.

Does this sound like your next challenge? Apply today!

Your Responsibilities

• Working in an industry-leading in vitro safety lab you will work with internal research groups to identify potential off-target risks for siRNA/antisense oligonucleotide (ASO) projects.
• Develop in vitro assays to explore those potential off targets in a variety of different mammalian cell types via gene expression analysis.
• You will also be required to summarize safety related literature relating to modulation of off-target genes to help inform decisions and support the development of safer oligonucleotide-based drug products.

The Bigger Picture

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 than 50 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.

Our Expectations

The ideal candidate has a passion for in vitro lab based experimentation and analysis and value the utility of early drug safety investigations. We are looking for someone with strong communication and collaboration drive, who can adopt a brave and forward-thinking approach to drive our predictive in vitro safety assay design to support drug discovery and development projects.

• PhD in biology, biotechnology, toxicology or pharmacology or a related field.
• Strong background in mammalian cell biology and in vitro work in molecular biology & omics including gene expression modulation via siRNA/ASOs and qPCR measurements. Additional in vitro techniques would be advantageous including fluidigm qPCR, high content cell imaging, western blot, ELISA & FACs.
• Experience of complex in vitro cell models or MPS systems would be desirable.
• Track record of scientific literature review with an ability to pull together various sources of data to inform on potential safety questions & targets of interest.
• Strong communication skills: including presenting, communicating data analysis, influencing and building partnerships with internal and external research groups.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

Seeking a Separation Scientist for the iLAB Team at AstraZeneca in Gothenburg.

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? We are seeking a specialized Separation Scientist that will play an important part in the iLAB team, focusing on the analysis and purification of chemical libraries. Welcome to AstraZeneca in Gothenburg!

Purpose, Offer and Benefits

This is a 1 year consulting assignment starting in september. You will  be employed by TNG during the assingment period.

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 recognize people are our greatest asset. Here we are dedicated to being a Great Place to Work .

Your Responsibilities

• 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 organization focused on innovation & project delivery; collaborating closely with scientists across the discovery organization

The Bigger Picture

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.

Our Expectations

You´re a separation scientist with a track record of applying innovative analytical chemistry solutions. You also have:

• BSc/MSc in Chemistry or Analytical Chemistry
• Good knowledge of analytical and/or preparative chromatographic techniques (HPLC, HPLC-MS) including method development and instrument troubleshooting
• Lab-based experience using analytical chemistry and/or automation techniques.
• Detailed understanding of the use of analytical techniques to solve complex scientific questions.
• Ability to work in multidisciplinary team / project / function.
• Excellent communication skills
• First-rate time management skills, forward planning, and delivery focus, leading to good team working and a high level of self and team delivery.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

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 specialized 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.

About the position
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
• 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 organization focused on innovation & project delivery; collaborating closely with scientists across the discovery organization

Your profile
You’re a separation scientist with a track record of applying innovative analytical chemistry solutions. You also have:

• BSc/MSc in Chemistry or Analytical Chemistry
• Good knowledge of analytical and/or preparative chromatographic techniques (HPLC, HPLC-MS) including method development and instrument troubleshooting
• Lab-based experience using analytical chemistry and/or automation techniques.
• Detailed understanding of the use of analytical techniques to solve complex scientific questions.
• Ability to work in multidisciplinary team / project / function.
• Excellent communication skills
• First-rate time management skills, forward planning, and delivery focus, leading to good team working and a high level of self and team delivery.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

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 consist of 7 teams spread across Sweden, UK and 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.

About the position
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 the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects..

Responsibilities
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that rapidly can 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

Your profile
-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 benificial.
Experience in lung research is desirible
- Excellent written and oral communication skills in English is a must

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

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 consist of 7 teams spread across Sweden, UK and 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.

About the position
As a 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 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 rapidly can become an integrated project member and deliver key data.

Responsibilities
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

Your profile
Essential requirements:
-A relevant science degree (MSc or BSc) ( 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 benificial.
- 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 organized and incorporate the views of others in your communication and collaboration.

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

About the position
We now offer a unique opportunity for senior scientist with great skills in peptide chemistry and with a special interest in bridging novel synthetic chemistry and medicinal chemistry in design of drug modalities and conjugates. Join our experienced team in New Modalities drug discovery and contribute with your high ambitions, collaborative mindset and enthusiasm. The position is placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden.

Responsibilities
The role is fully lab based and focused on synthetic chemistry of various modalities and drug conjugates, in particular peptide chemistry
You will actively contribute to compound design and synthesis, analysis, purification, data generation and data interpretation.
The person will need to be skilled in both oligonucleotide synthesis, oligo building block synthesis and oligo conjugate synthesis and has to have hands on experience with several oligo instruments.

Your profile
Essential for the role
We are looking for an ambitious team player that have expert knowledge in synthetic organic chemistry applied across multiple modalities and handling of complex molecules.
• Ph. D. degree in Organic Chemistry, Medicinal Chemistry, Chemical Biology with emphasis on peptide synthesis and oligonucleotide synthesis.
• Synthetic chemistry: ability to plan, prioritize and perform work independently including synthetic route design and problem solving
• Awareness of recent literature as well as current developments and trends in organic synthesis
• Highly self-motivated and capable of analyzing complex data and deciding on focused course of action
• Excellent teamwork, collaboration, networking and communication skills

About the organisation
This is a consultant assignement for one year at AstraZeneca in Gothenburg. Start day depends on when it is suitable for the candidate. During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

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



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



Drug Product Delivery (DPD) within PT&D is the internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.



Embrace an exciting opportunity at Drug Product Delivery (DPD) within PT&D, in a role as Delivery Lead.



In this role you are driving studies that are going to be packed in our internal assets and working closely with the project team to ensure studies are progressed according to timelines.

The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment.



What you'll do

*

Ensuring that DPD activities are scheduled, resourced and executed according to the study timelines.
*

Optimizing the design of high-quality clinical trial kits to ensure effective processes for packaging, labelling and distribution to ensure on time delivery to our clinical trials
*

Contributing to the overall improvement of DPD processes and capabilities.
*

Leading development and/or implementation for improvements of processes or equipment to increase efficiency and effectiveness within CM&S.
*

Participating in projects related to the internal packing facility.



Essential requirements for this role

* BSc/MSc in a relevant discipline or equivalent experience.
* Proven experience within pharmaceutical development.
* Good understanding of the principles, application and management of SHE and GMP in an R&D environment.
* Curious and innovative mindset with proven problem solving skills - able to resolve complex issues with minimal guidance
* Proven and demonstrated complex planning background
* Understanding of effective planning processes
* Project management background
* Proven strong digital skills
* Improvement mindset and track record of leading improvements



At AstraZeneca's Operations, we have a big ambition: to deliver more medicines to patients, quicker and more affordably. Backed by investment, leadership, and a clear plan to get there, we bring personal dedication and out-of-the-box thinking. We are driven by our commitment to deliver accelerated growth for AstraZeneca and to make people's lives better.



So, what's next? We welcome your application no later than May 29th, 2024. Visa mindre

We now have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.
Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

About the position
The DPD Operator role will be a operational role within Distribution one of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in an environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:
- Distribution experience from a complex supply chain organization
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Responsibilities
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused operational within Distribution. As a DPD operator you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and manage deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.
Distribution responsibilities example
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.

Your profile
Essential requirements:
-BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
-Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization
-Understanding of principles, applications and management of SHE and GMP in an R&D environment
-Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
-Good written and verbal English communication and understanding

Soft skills:
As a person, you should have a curious and innovative mindset with problem solving ability, resolving issues with minimal guidance. The perfect candidate should show interest in working operationally to learn and quickly adapt to the new tasks with a willingness to develop within this role.

About the organisation
This is a consultant assignement for one year util June 2025 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

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

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

Embrace an exciting opportunity at Drug Product Development (DPD) within PT&D, in a role as Delivery Lead.

At DPD, we are the internal asset for packing, labelling and distribution of our studies - next to external process. In this role, you are the internal asset representative in the decision meeting, selecting which studies are going to be packed in internal or external assets. All decisions are concerning capability and capacity on internal vs external assets and are taken in close cooperation with DPD LT. The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment.



What you'll do

* Manage the internal P&L planning process, working closely with internal but also external packaging and labelling.
* You will ensure that DPD activities are planned, resourced and executed according to the study timelines.
* Monitor and communicate capacity requirements to DPD LT
* You will also contribute to the overall improvement of DPD processes and capabilities.
* Participate in projects related to the internal packing facility.
* Lead weekly meetings with Delivery Leads

Essential requirements for this role

* Good understanding of the principles, application and management of SHE and GMP in an R&D environment.
* Curious and innovative mindset with problem solving skills - able to resolve complex issues with minimal guidance
* Proven complex planning background
* Understanding of effective planning processes
* Project management background
* Strong digital skills
* Improvement mindset and track record of leading improvements

At AstraZeneca's Operations, we have a big ambition: to deliver more medicines to patients, quicker and more affordably. Backed by investment, leadership, and a clear plan to get there, we bring personal dedication and out-of-the-box thinking. We are driven by our commitment to deliver accelerated growth for AstraZeneca and to make people's lives better.

So, what's next? We welcome your application no later than May 29th, 2024. Visa mindre

Senior Scientist Pharmaceutical/Senior Analytical scientists to Oral Product Development at AstraZeneca in Gothenburg

We now have the opportunity for a consultant to join the team in the role as Senior Scientist Pharmaceutical/Senior Analytical scientist within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg. Welcome with your application!

Purpose, Offer and Benefits

This is a consulting assignment starting in August and will continue until the end of December. You will be employed by TNG during the assignment period

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.

Your Responsibilities

We are looking for a senior 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 determining 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.

The Bigger Picture

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.

Our Expectations

 

• University degree (BSc, MSc, PhD) in relevant subject area, with industry experience
• Experience from working with chromatography and other techniques e.g. HPLC/UPLC, and dissolution, both in a GxP and a non GxP environment.
• Experience of supporting clinical manufacture and working with contract manufacturing organisations.
• Experience of authoring CMC content for the analytical aspects of drug product regulatory filings throughout the clinical development phase.
• Experience of the analytical area such as method development and method validation.
• Experience from evaluation of stability data and assigning shelf life to drug products.
• Excellent communication skills and a proven track record of working collaboratively to develop innovative solutions.
• Strong leadership skills including the ability to deliver robust scientific contributions to projects and utilise risk-based approaches to project delivery.
• Good knowledge in written and spoken Swedish and/or English is necessary.

To be successful in this role you will need expertise in analytical chemistry and an experience from laboratory work. Excellent skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

We are looking for an Analytical scientist Oral Product Development at AstraZeneca in Gothenburg.

Do you have scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques? We now have the opportunity to join the team in the role as Analytical Scientists within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg.

Purpose, Offer and Benefits

This is a consulting assignment starting in August and will continue until the end of December. You will be employed by TNG during the assignment period.

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.

Your Responsibilities

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 determining 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.

The Bigger Picture

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.

Our Expectations

• BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other disciplines with relevant skills.
• Scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.
• Experience from working within the pharmaceutical industry is an advantage.
• If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.
• Good knowledge in written and spoken Swedish and/or English is necessary.

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.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

About the position
We now have the opportunity for a consultant to join our team in the roles as Analytical Scientists within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg.

Responsibilities
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 determining 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.

Your profile
-BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other disciplines with relevant skills.
-Scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.
-Experience from working within the pharmaceutical industry is an advantage.
-If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.
-Good knowledge in written and spoken Swedish and/or English is necessary

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.

About the organisation
This is a consultant assignement from August until end of December 2024 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

About the position
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.

Responsibilities
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.

Your profile
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.

About the organisation
This is a consultant assignement from August until end of December 2024 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies – at AstraZeneca, we are proud to have a unique 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. Visa mindre

About the position
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.

Responsibilities
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.

Your profile
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.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

Om tjänsten
Vi letar efter en forskare inom analytisk kemi som kan bidra med sin expertis inom området analytisk vetenskap under utvecklingen av läkemedelsprodukter. Arbetsuppgifterna kommer att inkludera analytiska tester, dokumentation samt att delta i och hålla presentationer vid projektgruppsmöten. Rollen är primärt laboratoriebaserad.

Tjänsten är på heltid (100%) och förväntas starta i början av juni 2024, med planerat avslut den 31 december 2024. Det är viktigt att notera att detta är ett konsultuppdrag, vilket innebär att du kommer att vara anställd av oss på Poolia men arbeta ute hos kunden i Göteborg.


Vem är du?
För att vara aktuell för tjänsten behöver du som söker uppfylla följande krav:
- Kandidat- eller masterexamen inom farmaci, kemi eller analytisk vetenskap.
- Vetenskapliga kunskaper inom analytisk vetenskap, inklusive laboratorieerfarenhet med hantering av datoriserade system och kromatografitekniker för detektion av små molekyler.
- Goda kunskaper i svenska i både skrift och tal, och/eller engelska.

För att trivas och lyckas i rollen bör du vara välorganiserad, analytisk, flexibel och noggrann. Du trivs med att arbeta tillsammans i team och har förmågan att arbeta självständigt. Vidare bör du ha goda kommunikationsfärdigheter och vara van vid att arbeta inom snäva tidsramar.

Välkommen med din ansökan genom att registrera ditt CV. Urvalsprocessen pågår löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag.


Om verksamheten
Konsultrollen passar dig som på kort tid vill skaffa dig bred erfarenhet. Vi erbjuder dig chansen att arbeta på populära arbetsplatser med välkända varumärken där du kan utveckla din kompetens och bredda ditt CV. Du kommer att trivas som konsult om du söker en värld av spännande uppdrag och nya kontaktnät. Vid din sida har du din konsultchef som agerar bollplank och stöttar dig i att lyckas på dina uppdrag. Vi vill att du ska må bra och trivas med oss på Poolia. Därför erbjuder vi dig friskvårdsbidrag, rabatter på olika träningsanläggningar och ordnar regelbundet sociala aktiviteter. Självklart omfattas din anställning på Poolia av kollektivavtal, försäkringar, tjänstepension samt företagshälsovård. Visa mindre

Research Scientist position – in vitro cellular profiling to AstraZeneca in Gothenburg

Would you like to join the Mechanistic and Structural Biology department within the Discovery Sciences organization at AstraZeneca. We are looking for a motivated research scientist with a passion for applied science to AstraZeneca in Gothenburg.

Purpose, Offer and Benefits

This is a consulting assignment with a duration of 6 months. You will be employed by TNG during the assignment period. Please note that the selection is ongoing.

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 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.

Your Responsibilities

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.

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.

The Bigger Picture

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.

Our Expectations

• 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.

 

 

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

About the position
We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden.

Respiratory & Immunology is one of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD).

Responsibilities
As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

What you’ll do:

• As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

Your profile
• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R’s (reduction, refinement and replacement) across the full range of studies.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

Scientist In vivo Bioscience at AstraZeneca Gothenburg!

We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology at AstraZeneca in Gothenburg, Sweden. Respiratory & Immunology is one of AstraZeneca´s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD)

Purpose, Offer and Benefits

This is a 9-month consulting assignment starting in May. You will be employed by TNG during the assignment period. Please note that the selection process is ongoing.

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

Your Responsibilities

As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

• You will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

The Bigger Picture

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

 

Our Expectations

• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R´s (reduction, refinement and replacement) across the full range of studies.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

About the position
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.

Responsibilities
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.

Your profile
Requirements:

• Degree in pharmacy or engineering (specializing 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)
• Fluent in written and spoken English
• Experience of documentation, deviations, changes, and other quality and compliance decisions in the development projects.

Desirable:
• Experience preferably within a pharmaceutical manufacturing organization is desirable
• Understanding of Project Management processes
• Good team working 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
• Good communicator with experience of interacting effectively across interfaces.
• Comprehensive understanding of the pharmaceutical/drug development process

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

About the position
Do you have an interest in clinical supply chain and working with external vendors and are you a person who would like to be part of a truly global team and play a key role in getting medicines to patient – then join us!

Pharmaceutical Technology and Development (PT&D) apply science and technology that turns concepts into actual medicines which help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

Clinical Manufacture & Supply (C&MS;) within PT&D provides an agile and flexible end-to-end Clinical Supply Chain that manufactures, outsources and delivers supplies and services to hundreds of thousands of patients across the globe.

Responsibilities
CM&S are now looking for an External Supply Co-ordinator to join our global External Commercial Product Team in Oncology Therapy Area on a 12 month contract. We are seeking those who embrace change, show great initiative, flexibility, and a willingness to learn. As External Supply Co-ordinator, you will establish relationships with external suppliers and collaborate in teams of internal experts (e.g., Technical, Quality Assurance, Procurement) in the sourcing of services and goods required by CM&S from external suppliers in support of global projects for AstraZeneca. This role will have a specific focus on sourcing the goods and services required for sourcing commercially available product for use in AstraZeneca sponsored Clinical Trials. We would ideally like to receive applications from people with clinical supply chain and supplier management experience.

Your profile
Requirements for the role:

• BSc level education in a relevant discipline.
• Minimum 5 years’ experience of working within a Research & Development or Procurement environment and working with external providers.
• Appropriate depth of technical knowledge for the activity being sourced, to be able to fully understand any risks to delivery and make the best use of the technical experts on the team to make effective decisions.
• Experience of data analysis

Desirable for the role:

• Supplier Relationship Management skills
• Understanding quality principles and GMP requirements
• Project Management experience.
• Networking skills
• Good communication skills
• A high degree of personal credibility when interfacing with organisations internal and external to AZ.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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. Visa mindre

Clinical Pharmacology Expert (Director or Associate Director) in CVRM



Do you have expertise and experience in clinical pharmacology, PK, PKPD, Model Informed Drug Development (MIDD) and its application in drug development? Would you like to apply your expertise in a company that is following the science and turn ideas into life changing medicines? If yes, we have the position for you at AstraZeneca!



We now have an exciting opportunity for an engaged and diligent individual to join our growing Clinical Pharmacology and Quantitative Pharmacology (CPQP) team at AstraZeneca at our vibrant Gothenburg site in Sweden, as Associate Director or Director depending on your experience and skills.



This is a global role that will support large- and small molecule projects across all phases of clinical development within the therapy area of Cardiovascular, Renal and Metabolism.



We are a global, science-led BioPharmaceutical business and our innovative medicines are used by millions of patients worldwide. Within the Clinical Pharmacology and Safety Sciences (CPSS) function at AstraZeneca, we have a groundbreaking Clinical Pharmacology and Quantitative Pharmacology (CPQP) organization with a diverse and uniquely skilled team of clinical pharmacometricians, clinical pharmacology scientists and other experts. You will thrive in an energising environment where challenging work goes hand in hand with development. With opportunities, recognition and inquisitive minds, there's no better place to unlock learning and build a long-term career. Gothenburg is a key research and development location for our Cardiovascular, Renal and Metabolism area.



What you will do

Working closely with clinical pharmacometricians, physicians and other scientists, you will apply your expertise and leadership skills to contribute to the strategy of the clinical development program and the design and interpretation of clinical studies. You will influence key decisions in early and late phases of clinical development.



In collaboration with clinical pharmacometricians, you will represent CPQP in cross-functional project teams, and be responsible for developing the clinical pharmacology strategy. The work includes integration of relevant data, such as dose information, pharmacokinetics, biomarkers and clinical endpoints within and across studies, compounds and development stages. You will take part in finding opportunities to apply model informed drug development to accelerate and advise decision making. Based on your interest, skills and experience, you might also perform some pharmacokinetic and pharmacometrics modelling and simulation acting as a dual Clinical Pharmacometrician/Clinical Pharmacologist. You will communicate your findings within and outside of AstraZeneca and publish in peer reviewed journals.



Minimum requirements for the role

*

PhD in clinical pharmacology or other relevant area
*

Good knowledge of pharmacokinetics, PKPD and Clinical Pharmacology
*

Biological understanding of disease and drug action
*

Good oral and written communication skills



Desirable in the role

*

3+ years of industry experience or equivalent in pharmacokinetics and clinical pharmacology in drug development
*

Track record in creating and delivering on clinical pharmacology strategies of both small and large molecules
*

Early and late phase clinical development experience
*

Good knowledge and experience in use of PK and PKPD modelling and its clinical application
*

Recognized clinical pharmacology expertise as demonstrated by scientific publishing in the field of clinical pharmacology



We truly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues, mentors and leaders, will ensure you maximise your skills, abilities and contribution. You have a real passion for your subject, along with a collaborative nature and ability to work in multi-disciplinary global teams.



Why AstraZeneca?

We are a global, science-led BioPharmaceutical business and our innovative medicines are used by millions of patients worldwide. Collaborate in an inclusive environment, a place full of bold new opportunities. Be empowered to be innovative and creative where difference is valued.


So, what's next! Does this sound like your next challenge? Apply today!



We look forward to find out more about you. Send in your application as soon as possible as we will review applications continuously.


For more information about the position please contact the hiring manager, Angelica Quartino (https://www.linkedin.com/in/angelica-quartino-352a7b2/)



Where can I find out more?

Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Life in Gothenburg site: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.html
Read more about BioPharmaceuticals R&D: https://www.astrazeneca.com/r-d.html
Follow AstraZeneca on LinkedIn: https://www.linkedin.com/company/1603/ Visa mindre

We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that are following the science and turn ideas into life changing medicines.

We have an exciting opportunity for a Team Manager Drug Product Delivery to join our Drug Product Development team within our Clinical Manufacturing & Supply department in Gothenburg, Sweden.

Drug Product Development (DPD) is the only site within AstraZeneca that packs, labels and distributes investigational medicinal products to clinical trial patients around the globe. We support launched, pre-launch and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.


Main duties and responsibilities
As a Team Manager in DPD you will drive and develop planning, packing, labelling and distribution of drug product for clinical studies. You will have an impact on the speed, quality and cost of the AZ development portfolio. You will work in close collaboration within all DPD departments, Clinical Manufacturing & Supply and external Pack & Label.

Accountabilities include, but are not limited to:

* Leading, managing and developing a highly motivated team
* Providing supportive leadership and clear directions to the team, especially during periods of change
* Responsible for performance management of the team and individuals by ensuring individual objectives and development plans are aligned with AstraZeneca values, behaviours and business needs
* Incorporating complex, broad understanding of scientific issues into plans and strategies to capitalize on ideas and initiatives that will drive success for your area now and in the future according to trends in the industry
* Ensuring GMP and SHE standards are upheld; ensuring AZ Policies and Standards are understood and followed
* Responsible for ensuring that the GMP facilities are operated in accordance with AstraZeneca and external regulatory policies and standards. Secure License to Operate
* Leading complex projects e.g. continuous improvement/forums or segments of large cutting-edge international projects, applying specialist knowledge
* May act as DPD Project leader within the agreed project portfolio, the role holder ensures the delivery of studies to agreed project plan


Essential Requirements

* MSc/BSc or equivalent experience in a scientific field related to the role
* Thorough understanding of GMP and SHE requirements
* Demonstrated ability to work with teams in a culturally diverse, complex and changing environment
* Project management experience
* Experience of leading and managing teams of people
* Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global environment
* Proven leadership, promoting motivation and empowerment of others in order to accomplish individual, team and organisational objectives
* High level of interest in the introduction and further development of digital process improvements.
* Excellent communication and strategic influencing skills across interfaces of discipline, culture and expertise both internally and externally

We see that the successful candidate enjoys problem solving and managing change in a positive approach to the challenges of change for self, team and the business. We assume that you have excellent networking and team working skills.


Why AstraZeneca

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

So, what's next? We welcome your application no later than March 27th, 2024. Visa mindre

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

Our team is growing, and we are now looking for two motivated individuals with experience in Biologics and/or small molecule drug development and PKPD, to join us as a DMPK Project Leader, from candidate selection to registration and beyond. These positions are placed at AstraZeneca's dynamic R&D site in Gothenburg, Sweden.

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

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

It is your responsibility to ensure delivery of all DMPK related activities throughout the value chain in accordance with regulatory requirements. These include preclinical PK experiments, in vitro ADME and biotransformation to yield pharmacokinetic understanding. Furthermore, assisting design of pharmacodynamic studies that ultimately delivers a pharmacological assessment underpinning human dose prediction and emerging clinical experience.

You will work as the development DMPK representative on project teams from candidate selection to registration and beyond. We believe that you have a solid understanding of DMPK, a working knowledge of pharmacology, and that you will be able to provide expert advice and interpretation of complex nonclinical and clinical data.

Main duties and responsibilities;

*

Communicate scientific progresses both externally and internally
*

Deliver DMPK input and data to projects within agreed timelines and to the right quality
*

Responsible for delivering and produce the nonclinical pharmacokinetic documentation to support clinical progression
*

Apply an understanding of DMPK to support/influence compound profiling, project progression and project strategy
*

Define and deliver a translational quantitative PKPD strategy in projects, so that effective conclusions can be made
*

Contribute to estimation of safety margins and report results and interpretations to project teams and internal governance bodies
*

Responsible for leading, coordinating and engaging with R&I DMPK colleagues in project related activities
*

Prepare clear presentations related to the above for internal governance bodies



Your level of professional experience will be relevant for your initial career level (Associate Principal Scientist or Principal Scientist).



?Essential for the role

*

PhD or equivalent experience in a relevant field
*

Expert in DMPK sciences with profound knowledge of drug discovery and development processes
*

Broad experience in biologics drug development (PK & Bioanalysis)
*

Have PK modelling skills, experience of human PK and dose prediction, as well as an understanding of disease biology and PKPD
*

Experience with regulatory submissions for biologics and/or small molecules
*

Knowledge of all DMPK assays including the use of in silico tools for PK prediction
*

Experience in project leadership
*

Collaborative mindset
*

Team player
*

Proactive in providing expert support to project team and excellent communication skills



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

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

What's next!
If you are ready to make a difference - apply today, and we'll make it happen together! We welcome your application until March 31, 2024. For more information about the position, please contact recruiting manager Lassina Badolo at [email protected]

Where can I find out more?
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Life in Gothenburg: https://www.movetogothenburg.com/
Culture and atmosphere of the Gothenburg site: https://www.linkedin.com/feed/update/urn:li:activity:6496327311678410752/
Relocate to Gothenburg: https://www.astrazeneca.se/om-oss/verksamheten-i-sverige/goteborg/relocate-to-gothenburg.html Visa mindre

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

We’re looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) at AstraZeneca 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.

Purpose, Offer and Benefits

This is a consulting assignment scheduled to commence in April and is expected to run until the end of December. You will be employed by TNG throughout the duration of the 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.

Your Responsibilities

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.

The Bigger Picture

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".

Our Expectations

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

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

We now have an exciting opportunity for a talented DPD Operator to join AstraZeneca in Gothenburg.

If you have a curious and innovative mindset with strong problem-solving abilities and understand Drug Product Delivery, Supply Chain, and Pharmaceutical development, then this role might be for you. We are currently seeking a talented Drug Product Delivery Operator to join AstraZeneca in Gothenburg!

Purpose, Offer and Benefits

This is a 1-year consulting assignment starting in May. You will be employed by TNG during the assignment period.

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.

Your Responsibilities

The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused operational within Distribution. 

You will:

• perform and document all the operational work according to written procedures
• be engaged in the development and improvement of internal processes and manage deviations
• be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas

Distribution responsibilities example:

• preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies

The Bigger Picture

Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas.We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

The DPD Operator role will be a operational role within Distribution one of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in an environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:

• Distribution experience from a complex supply chain organization
• Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Our Expectations

• BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
• Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization
• Understanding of principles, applications and management of SHE and GMP in an R&D environment
• Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
• Good written and verbal English communication and understanding

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre

Senior Scientist in Genome Engineering at AstraZeneca in Gothenburg.

We are looking for a new team member to join our Screening and Automation team in Genome Engineering Department. The role is based at AstraZeneca 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. If this sounds like your next challenge – welcome to apply!

Purpose, Offer and Benefits

This is a consulting assignment for approximately 9 months, starting in April. You will be employed by TNG during the assignment period.

Here at AstraZeneca, we are working towards turning novel state-of-art technologies into effective and safe medicines for severe genetic disease. 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.

Your Responsibilities

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.

The Bigger Picture

We 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.

Our Expectations

• PhD degree in molecular/cell biology, genetics or relevant areas, or MSc with 2+ years´ experience in academia or industry
• Strong molecular biology background and relevant hands-on skills.
• Expertise with mammalian cell culture and cellular assays, such as genetic manipulation
• and evaluating genetic & functional outcomes using next generation sequencing, qPCR etc.

Desirable for the role:

• Solid understanding of genome engineering and current technologies.
• Experience with automation and high-throughput application
• Experience with producing and using viral vectors (lenti/AAV) for gene delivery in mammalian cells.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter. Visa mindre