Senior Scientist in vitro ADME

AstraZeneca AB; Sweden; On-site; SEK 600,000 - 800,000; Full time

Job summary

AstraZeneca AB is seeking an ADME senior scientist in Gothenburg, Sweden, to enhance their in-vitro ADME capabilities. This role requires a PhD or MSc and offers the opportunity to work collaboratively on drug discovery.

The successful candidate will design and conduct studies, communicate findings effectively, and contribute to scientific strategies within cardiovascular, renal, and metabolism research.

Qualifications

• PhD or MSc with relevant experience post-graduation.
• Good knowledge of ADME processes and in-vitro models.
• Broad laboratory proficiency in molecular biology methods.

Responsibilities

• Design and conduct in vitro ADME studies using established protocols.
• Work independently on experimental design and analysis.
• Communicate data and guidance clearly to project teams.

Skills

ADME processes knowledge

Laboratory proficiency

Strong communication skills

Collaborative abilities

Education

PhD or MSc in relevant field

Tools

LC-MS

qPCR

Job description

Overview

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.

We are recruiting for an ADME senior scientist to join the DMPK&BBA department within Research and Early Development Cardiovascular, Renal and Metabolism (CVRM). You will strengthen our -vitro ADME team and increase our capabilities regarding in-vitro ADME, across all drug modalities.

CVRM is one of the three main therapeutic research areas within AstraZeneca which deliver candidate drugs into clinical development. CVRM DMPK is based in AstraZeneca’s world-class vibrant R&D center, located in Gothenburg, Sweden. DMPK interacts with other functions in supporting CVRM projects along the value chain, from target selection all the way to launch and life cycle management.

Responsibilities

ADME (Absorption, Distribution, Metabolism and Elimination) scientists work with all aspects of drug disposition, stretching from tissue exposure to subcellular drug handling, and relating to drug effects. We are accountable for the breadth of the CVRM drug portfolio. This laboratory based scientific role delivers high-quality data and scientific insights aligned with project needs. The role requires effective communication to provide clear data and guidance to project representatives, oversee externalised studies, and contribute to DMPK scientific strategy. The position requires sound scientific judgement about DMPK information sets, innovative problem-solving and cross-functional collaboration.

Main Duties and Responsibilities

• You will design, conduct, interpret and report in vitro ADME studies using established protocols and bespoke designs, applying state-of-the-art techniques, including e.g. 3D cell cultures, to support drug discovery and development. Additionally, you will provide oversight of outsourced studies and work with contract research organizations (CROs).
• You will work independently on experimental design and analysis, while incorporating input from colleagues. You will identify and implement technology improvements to achieve scientific and business goals.
• You will stay current with scientific advances, applying new knowledge to your projects and sharing insights with colleagues. You will suggest improvements in approaches, equipment, or techniques
• You will communicate data and guidance clearly to project teams, contributing to overall team delivery and planning all work to Good Laboratory Standards (GLS).
• You write manuscripts and publish research with internal and external collaborators, building your scientific profile.
• You may participate in cross-functional workstreams, lead the development and implementation of DMPK scientific strategies, and contribute to DMPK scientific strategy discussions within AstraZeneca.

Essential Requirements

• A PhD, or MSc with relevant experience post graduation
• Background in Pharmacy, Biology, Biochemistry, Medical Biosciences or related subject area.
• Good knowledge of ADME processes and in-vitro models of drug disposition, with experience in development, characterization and application of translatable in-vitro models
• Broad laboratory proficiency in e.g. handling and culturing primary human hepatocytes and other human cells/tissues, molecular biology methods, image analysis, and enzyme / transporter kinetic studies
• Strong communication skills in English, both verbal and in writing
• Collaborative abilities and team-player to engage across boundaries with a problem-solving approach and focus on delivery.

Desirable Requirements

• Industry experience
• Expertise in bioanalytical techniques, e.g. LC-MS, qPCR, and PCR
• Experience with automation equipment and automated processing

Additional information

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

We welcome your application (CV and Cover Letter) no later than 16th August, 2026! Please expect communication after advert closing date.

Date Posted 26-juni-2026

Closing Date 12-juli-2026

Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.