Jobs in Exeter

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves leading technical operations and providing strategic support for the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, collaborating with external manufacturing partners, and ensuring compliance with GMP standards and continuous improvement initiatives.

GSK United States

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. You will craft integrated therapeutic area strategies, combining clinical, scientific, and commercial insights to shape portfolio choices and investment priorities.

AstraZeneca London, United Kingdom

On-site Permanent

Vice President, Real World Evidence (RWE)

Your work will change lives. Including your own.The Impact You’ll Make:Recursion is currently seeking a seasoned leader to join our team as Vice President, Real World Experience. This role will lead RWE generation across the Recursion portfolio. The role will...

Recursion United Kingdom

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and interfacing with cross-functional teams and health authorities. The position requires a Ph.D., M.D., or Pharm D. with 5-9+ years of experience in drug development, proficiency in modeling software, and strong collaboration skills.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Lecturer (Above the Bar) in Environmental Microbiology & Biotechnology

The role involves conducting research and teaching in environmental microbiology and biotechnology, with a focus on areas like fungal biotechnology, synthetic biology, and microbial physiology. The appointee will contribute to teaching programs and develop a dynamic research program, particularly within the SUSFERM Future Strategic Research Centre.

University College Cork Cork - Ireland, Republic Of Ireland, United Kingdom €79,976 – €103,575 pa

On-site Permanent

Graduate Instrumentation Engineer

This role involves hands-on work in assembling, testing, and maintaining diagnostic equipment, as well as troubleshooting and supporting quality and validation activities. The graduate will work closely with experienced engineers and scientists, gaining exposure to cutting-edge healthcare technology and future product development.

HCL International Stevenage, Hertfordshire, United Kingdom £30,000 – £40,000 pa

On-site Permanent

Systems Engineer - Embedded and Hardware

This senior role involves leading the electronics and software workstream for IVD medical devices, ensuring robust system architecture, supplier governance, and regulatory compliance. The Systems Engineer will work closely with in-house teams and international suppliers, shaping architecture, design controls, and verification strategies.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent