Hays AB jobb i Göteborg

Experienced SAP S/4HANA EWM Consultant to lead in designing, building, and configuring SAP EWM applications

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

Role Overview
Our client is looking for an experienced SAP S/4HANA EWM (Extended Warehouse Management) Consultant who will take the lead in designing, building, and configuring SAP EWM applications. The role requires deep hands?on expertise across warehouse configuration, integrations, and end?to?end warehouse processes.

Key Responsibilities

* Take a lead role in the design, build, and configuration of SAP S/4HANA EWM applications
* Design and configure SAP EWM warehouse structures and processes
* Drive and support EWM solution design across inbound, internal, and outbound warehouse operations

Required Skills & Experience

* SAP EWM Configuration (Extensive Experience Required)

* Extensive hands?on experience configuring SAP EWM warehouse setup, including:
* Storage types
* Storage sections
* Activity areas
* Search sequences
* POSC (Packaging Specifications)
* LOSC (Layout?Oriented Storage Control)
* Slotting
* Replenishment
Handling Units & Warehouse Processes

* Strong experience with multi?level Handling Units (HUs) across:
* Inbound processes
* Storage
* Staging
* Outbound processes
SAP EWM Integrations & Execution

* Proven experience with:
* SAP EWM RF transactions
* EWM-PP integration, including PMRs (Planned Manufacturing Receipts)
* EWM-QM integration
Warehouse Process Knowledge

* Very good working knowledge of end?to?end SAP EWM processes, including:
* Inbound warehouse processes
* Outbound warehouse processes
* Internal warehouse processes
As part of the recruitment process, the client will conduct background checks on candidates who progress to later stages.

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

AI Research engineer - 15 months consultant assignment - AstraZeneca

Are you a machine learning engineer or scientist excited by building and scaling modern AI systems for real-world impact? Do you want to enable the training and inference of large-scale deep learning models for drug discovery? We are seeking a 15-month consultant to join the innovative MolecularAI department at AstraZeneca in Gothenburg, Sweden.

Our vibrant Gothenburg site brings together more than 2,900 employees from over 50 countries, creating a truly inspiring and collaborative environment. Here, history and scientific breakthroughs unite to drive new discoveries. We believe the diversity of our team is essential for turning bold ideas into reality.

At AstraZeneca, your engineering skills will directly influence our technology platforms and help shape the next generation of transformative medicines. Are you ready to make a difference? Join us and be part of our journey.



What You'll Do

You will drive impact across multiple projects with a focus on AI engineering and platform development. Your responsibilities will include:

* Optimize the training and inference of large-scale deep learning models for drug design on state-of-the-art HPC platforms

* Design, conduct and evaluate scientific experiments together with our multi-disciplinary research team to help us build the next generation of foundational chemical models.

* Extend and maintain scientific codebases written in Python that forms the backbone of our AI platforms. See https://github.com/molecularai/

* Collaborate cross-functionally with researchers in data science, software engineers and drug discovery domain experts

This is an on-site role based in Gothenburg, Sweden where you expect to present on site three days per week.



Essential Qualifications

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

* Degree in computer science, engineering, chemistry, physics, mathematics or related discipline, or equivalent industry experience

* Hands-on experience training models with PyTorch or equivalent frameworks

* Excellent programming skills, preferably in Python. Track record of developing sizable software solutions and familiarity with scientific packages (Numpy, Pandas, etc.)

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



Desirable requirements

You would benefit from having experience or familiarity with:

* Experience with high-performance computational platforms and schedulers such as SLURM

* Experience writing ETLs for large data sets

* Background in life sciences or physical sciences

* Research and outreach contribution to open-source projects, publications, or participation in online communities



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.

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

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

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

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

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

What will you do:

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

Your accountabilities will include:

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

Why AstraZeneca?

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

About Hays

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

Drug Product Delivery Operator - Consultancy Assignment in Gothenburg

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

What you will be working with

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

You will be part of a team specialising in:

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

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

Your core responsibilities:

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

Who we are looking for

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

Essential qualifications:

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

Beneficial skills:

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

What you can expect

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

Ready for your next step?

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

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

About Hays

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

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

Formulation Scientist - 10 month assignment - AstraZeneca

Do you have knowledge in pharmaceutical formulation development, with a practical understanding of design of experiments (DOE), material properties, and data curation and processing? Would you like to apply your expertise to link materials properties to process performance in continuous manufacturing? Then AstraZeneca might be the place for you.

AstraZeneca is a global, innovation driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. We are currently seeking a consultant Formulation Scientist to join our team within Global Product Development (GPD), part of Pharmaceutical Technology & Development (PT&D), in Gothenburg, Sweden.

You bring fundamental scientific understanding of formulation science and hands on laboratory experience, with the ability to work independently and contribute in cross functional development settings.

In PT&D, we are the bridge between science and innovative medicines that help millions of people. We design and deliver active ingredients, formulations and devices required to support new medicines-from supplies for use in early toxicology studies and clinical trials to developing technology to enable scale up for commercial manufacture. At GPD we focus on oral, inhaled, and parenteral drug products, playing a key role in the development of new medicinal products.

What you'll do:

This role is laboratory based and you will work in cross functional, cross skilled pharmaceutical development teams, contributing to sub teams to deliver key results related to formulation design and process performance.

In this role you will:

* Analyse and evaluate material properties and their impact on formulation and process performance, using experimental studies and basic data processing.
* Plan, set up, and run feeder trials across different settings and configurations, linking powder properties to continuous manufacturing behavior.
* Curate, acquire, and process experimental data; perform basic analyses (trends, variability) and maintain traceable records (ELN/Excel) with good documentation practice.
* Work safely and compliantly: conduct risk assessments, use PPE, handle powders/chemicals safely, and adhere to SOPs.
* Collaborate in a multi experiment environment, communicating clearly and managing time to meet project timelines.

You will typically have:

* Hands on experience executing formulation and process experiments, with enthusiasm for laboratory based work and independent operation.
* Basic knowledge of DOE, materials characterization, and data processing/visualization, with interest in linking material-process-performance.
* Collaborative communication skills and an agile mindset, with the ability to adjust to dynamic project demands to meet project and patient needs.

Why AstraZeneca?

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

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

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

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

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

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

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

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

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

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

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

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

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

What you will do:

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

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

In this role you will:

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

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

* Provide experimental support to project teams.

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

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

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

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

Why AstraZeneca?

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

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

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

Animal Technician - AstraZeneca - Gothenburg - 6 month consultancy assignment

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

The arena:

Animal Technician

AstraZeneca is a global, innovation-driven biopharmaceutical company that focusses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. We are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

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

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

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



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

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



What you need to do now

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

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

Senior Scientist - NGS Molecular Biologist - AstraZeneca - Gothenburg - 12-month consultancy assignment

NGS Molecular Biologist - Oligonucleotide therapies

Are you an experienced scientist with great expertise in Next Generation Sequencing and Molecular Biology? Do you want to use this expertise to contribute to the discovery of novel oligonucleotide therapies? We have an opening suitable for you!

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

AstraZeneca's ambition is to become world-leading in in the field of oligonucleotide therapies. We are achieving this through advances in oligonucleotide science and innovation internally and through the establishment of key collaborations outside AstraZeneca. To this end, we currently have a portfolio of very high-profile projects at different phases of drug discovery within AstraZeneca, and you will directly contribute to their successful progression to oligonucleotide therapies.

What you will do:
This lab-based role is for a Molecular Biologist with significant NGS expertise, which you will apply to the characterisation and profiling of the effects of oligonucleotide treatments in in vitro and in vivo cellular assays and models in support of novel drug discovery projects.
Our team is a collaborative group, and you will engage in the supervision and mentorship of other scientists, ensuring that methods run expertly and accurately, developing and guiding the setup of new techniques. Included in the role is also to nurture strong collaborative relationships with the project investigators, key partners, and data scientists to ensure the smooth running of projects.



Essential for the role:
* Ph.D. degree or MSc with corresponding experience in a relevant scientific discipline.
* Hands-on lab-based experience in utilising advanced molecular biology RNA-sequencing techniques.
* Experience covering all relevant aspects from hypothesis generation, through experimental design and execution, large-scale RNA and DNA extraction, sample and library preparation, sequencing, data handling, post-sequencing QC, and troubleshooting.
* Experience in the detection of nucleic acids in high-throughput assays and approaches.

Desirable for the role:
* Working with laboratory automation / liquid handling systems, method and technology development and optimisation.
* Knowledge of Oligonucleotide therapies (siRNAs and/or ASO)
* Hands-on laboratory experience running NGS platforms (Illumina, Oxford Nanopore etc).
* Sample Tracking by LIMS systems.

You should also have the ability to communicate, interact, and collaborate with your direct team members, as well as across our global AZ 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 molecular biology RNA-sequencing techniques.

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



What you need to do now

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

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

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

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

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



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

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

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

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



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



What you need to do now

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

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

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

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

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

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

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

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

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

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

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

Start date: 15/8 2025

So, what's next?
Are you ready to bring innovative ideas and fresh thinking to the table? Then you might be the person we are looking for!

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



What you need to do now

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

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

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

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

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

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

Benefits:
* Opportunities for continuous professional development and training.

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

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

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

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

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



What you need to do now

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

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

Senior Design Researcher - AstraZeneca/Evinova - Gothenburg - 12-month consultancy assignment

The Evinova Design team enables better experiences and outcomes for patients and researchers by crafting digital solutions for clinical trials. Design is central to our innovation process, from opportunity identification and early-stage idea generation, through detailed design of digital solutions, until adaptation and scale-up within clinical studies.

As a Senior Design Researcher, you will be part of the research and human factors team, responsible for the human insights that inspire and inform our products. Our work spans from foundational and generative research that informs early-stage innovation, to evaluative research and in-market experiments that drive continuous improvement. Drawing on a broad toolkit of qualitative and quantitative methods, we select those that are most relevant to the strategy and design choices we need to make. We work at pace across multiple initiatives, while maintaining methodological and ethical integrity.

As internal champions for human-centred design, we help build capability, involve cross-functional teams in the research process, make research insights systematically available and usable, and continuously evolve our research toolkit.

On a typical project you will:
* Scope the required research activities based on a deep understanding of the project goals, business requirements, underlying scientific foundations, and enabling technologies.
* Plan and conduct foundational, generative, and evaluative research.
* Synthesise research outcomes into impactful models and frameworks - such as archetypes, journeys, and user requirement specifications.
* Contribute to an expansive, interdisciplinary research practice that takes advantage of the varied perspectives and contributions of our product, technology, data, strategy, and science teams.



Requirements:
* Five to 10 years of professional experience doing research in a product or service design context, preferably in healthcare or life sciences
* Proficiency in human-centred design methods, familiarity with agile design principles and ways of working
* Affinity with Evinovas/AstraZeneca's values, and a passion for crafting digital health solutions that combine the best of design and science
* Strong collaboration, presentation, and storytelling skills
* Willingness to travel for research, project delivery, and client meetings

Desirables:
* Experience in healthcare and/or digital health
* Non-linear career paths and diverse life experiences that enrich your perspective
* Familiarity with clinical trials and the drug development lifecycle
* A second language (and every additional language is a plus!)



Start date: 2nd June

Join Evinova and help enable global life sciences to accelerate better health outcomes.



What you need to do now

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

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

Senior Research Scientist - NGS based Proteomics Specialist - AstraZeneca - Gothenburg - 12-month assignment

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

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

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

In this role you will:
* Utilise prior practical laboratory experience in transcriptomics/proteomics data generation with a strong emphasis on automation technologies.
* Contribute to planning and execution of projects involving new omics technologies, integrating automated solutions to enhance efficiency and precision.
* Develop and implement innovative automated processes to streamline the workflows.
* Maintain laboratory processes and equipment rigorously, ensuring efficient operation and performance of automated systems and workflows.
* Provide experimental support to fellow team members, promoting a collaborative environment and help implementing high-throughput workflows.
* Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca's corporate responsibility policies.
* Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.
* Collaborate with a wide range of scientists from different backgrounds to ensure the highest quality of research.
* Develop and validate cutting-edge protocols for the simplification of multiomic research through automation.



Essential for the role:
* Master's degree or higher in a relevant scientific discipline and/or equivalent demonstrated experience in a relevant academic or industry environment.
* A strong understanding of molecular biology theory and techniques.
* Hands-on experience with at least one Next Generation Sequencing/Transcriptomics/Proteomics technology (NGS-based proteomics technology, RNA-seq, DNA-Seq, Genotyping methodologies, mass spectrometry).
* Experience with automation technologies and integrating them into routine laboratory practices.
* Excellent organisational and communication skills.

Desired Qualifications:
* Extensive research experience in Pharma/Biotech, medical, or academic environments.
* A record of high-quality peer-reviewed publications or scientific presentations.
* Experience in laboratory automation utilising automated liquid handlers or scheduling engines.
* Experience of operating in a regulated environment such as GLP or ISO15189
* Demonstrated expertise in statistics, quantitative data analysis, data mining, and familiarity with LIMS (Laboratory Information Management Systems).

Start date: 2nd June.

If you are interested, apply now!

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

Quality Assurance Specialist - AstraZeneca - Gothenburg - 12-month consultancy assignment

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

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Senior Specialist with GMP focus for our Gothenburg team.

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

We have an exciting opportunity for a 12-month temporary assignment as Senior Specialist in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chains.

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

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

The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.

Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardize and simplify our internal processes.

Typical Accountabilities:
* Responsible for quality release of manufactured Drug Product, Investigational Medicinal Products for clinical trials.
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in development projects related to drug products.
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support the 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.



Essential for the role:
* M.Sc. in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment (manufacturing, packaging or analysis).
* Demonstrates an understanding of international quality systems regulations, concepts, and industry practices to adopt best-in-class processes.
* A comprehensive understanding of GMP regulations, the pharmaceutical development process and the supply chain process would be advantageous.
* Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and a "can-do" attitude.
* Excellent teamwork and networking skills and encourages team effectiveness.
* A good communicator with experience of interacting effectively across interfaces, collaborating internally.
* Fluent in written and spoken English.

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



What you need to do now

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

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

Formulation/Analytical Scientist - AstraZeneca - Gothenburg - 12-month consultancy assignment

Formulation/Analytical Scientist, Pharmaceutical Sciences

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

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".

Are you an enthusiastic, innovative, and motivated Formulation/Analytical Scientist seeking a unique opportunity? Join our small molecule formulation team in Advanced Drug Delivery at AstraZeneca's vibrant R&D site in Gothenburg, Sweden. We offer the experience to collaborate with dedicated team members and to work closely with other skill experts delivering AstraZeneca's early portfolio.

Responsibilities:
This is a lab-based role where you will support several drug project teams and provide your technical and scientific expertise in formulation development. You will develop and deliver different formulation systems for oral, inhaled and parenteral use, with a focus on liquid formulations. You will also perform essential characterisation work e.g. content, stability, homogeneity, impurity, pH, and particle size measurements, supporting projects in the discovery and preclinical development phase. The role requires close collaboration with other internal functions to further build our capabilities within advanced drug delivery.

You are expected to perform lab-based experimental work in accordance to project timelines, appropriate Safety, Health & Environment (SHE), quality and compliance standards, and in close collaboration with other formulators and analysts, as well as other skill experts (solid state and biopharmaceutical experts). The work should be documented carefully and to the right quality and standard, and clearly communicated to your project team.

Requirements:

* MSc degree in a scientific discipline relevant to analytical and formulation science (e.g., chemistry, pharmaceutical technology, or equivalent qualifications).
* Basic understanding of liquid formulations and basic knowledge of analytical methodologies such as spectrometry and separation science (U/HPLC).
* Genuine interest in experimental work and hands-on problem-solving.
* Delivery focused with the ability to utilise scientific and innovative thinking.
* Great communication skills in English, both orally and in writing.

Desirable skills/experience:
* Technical competence in the field of drug product formulation development for oral and/or parenteral delivery.
* Experience in working with formulation development or similar product development, or other laboratory skills of relevance.
* Good understanding of suitable quality standards and regulatory frameworks

If your passion is science, and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be. Join us at AstraZeneca, where we truly understand science and apply it every day to strengthen and grow our pipeline.

What you need to do now

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

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

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

Associate Director Validation, site Quality

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

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

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

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

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

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

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



What you need to do now

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

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

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

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

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

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

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

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

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

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

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

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

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



What you need to do now

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

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

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

Flow cytometry Senior Scientist in the Microphysiological Systems (MPS)

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

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

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

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

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



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

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

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



What you need to do now

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

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

Scientist EPDM - AstraZeneca - Gothenburg - 6 month assignment

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

Scientist - Early Product Development and Manufacturing

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

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

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

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

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



What you need to do now

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

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

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

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

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

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

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

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

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



What you need to do now

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

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

Analytical Chemist - AstraZeneca - Gothenburg

Hays is currently recruiting for an Analytical Chemist for a 12-month consultancy assignment.

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

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, manufacturing of Active Pharmaceutical Ingredients (API) and Investigational Medicinal Product (IMP) across all the AstraZeneca therapy areas. Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".

We're looking for a talented and motivated Analytical Chemist (Scientist/Senior Scientist) to join our analytical characterisation team within Early Product Development and Manufacturing (EPDM) in Gothenburg, Sweden.



What you'll do:
In the role as Scientist/Senior Scientist, you would join a highly collaborative team, and together we will deliver the analytical science to drug product development within the early portfolio up to phase II. To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus. This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality, as well as contributing to regulatory clinical trial applications (CTA). You will get the opportunity to apply your excellent analytical expertise in the drug product projects you will be working in. You will contribute to the progress of drug product development, getting new medicines for patients and driving the scientific development within the field of analytical science at AstraZeneca.

Essential requirements:
- 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
- Broad industry experience of pharmaceutical development including oral solid dosage form development
- Experience of CMC regulatory submissions and work according to GMP
- In-depth skills in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc.
- Excellent written and oral communication skills in English are a must
- Experience, knowledge and keen interest in the field of automation, AI and digitalisation would be advantageous
- Proven track record in publications related to analytical science or characterisation of pharmaceuticals is desirable

Soft skills:
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 in accordance with project timelines.
You keep abreast with the scientific discipline and the ability to drive and lead science and innovation personally, within the department and manage external collaborations to meet future needs.
You have excellent communication, collaboration, networking and leadership skills & the ability to lead and inspire colleagues.

At AstraZeneca, we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Here, we think holistically about patients and are always learning from those living with diseases. We harness digital, data science & AI to fast-forward our research, ensuring that work born in a lab can make a real difference. Every day, we impact patients' lives across the world.



What you need to do now

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

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

Solid State Scientist/Senior Scientist - AstraZeneca - Gothenburg

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

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

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

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

Accountabilities/Responsibilities

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

What you need to do now

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

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

Material Management and Distribution Operator - AstraZeneca - 9 month assignment - Gothenburg

Consultancy role for AstraZeneca.

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

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 is following science and turn ideas into life-changing medicines. We have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.

About the role:
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 of two Drug Product Deliveries in 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 in early phase clinical trials. To complement our existing team, candidates with the following experience are of interest:

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

Main Duties and Responsibilities
The role holder will contribute to the DPD organisation applying their expertise in the complex and regulated GMP environment. The work is focused on 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 managing 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.

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 organisation.

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

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



What you need to do now

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

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

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

Consultancy role for AstraZeneca

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

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

What you will do:

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

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

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

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

Why AstraZeneca?

When we see an opportunity for change, we seize it and make it happen, because any opportunity can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey in finding new ways to work, pioneering cutting-edge methods and bringing unexpected teams together!

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