Jobs in Exeter

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Director, Search & Evaluation Early TA Lead

Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Therapeutic Area Leadership Team (TALT), these leaders will identify and advance high-potential assets from preclinical...

CSL

Director, Search & Evaluation Early TA Lead

Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Therapeutic Area Leadership Team (TALT), these leaders will identify and advance high-potential assets from preclinical...

CSL

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Regulatory Affairs Intelligence Director

This role involves translating regulatory intelligence into strategic decisions that accelerate drug development and improve patient outcomes. You will work closely with senior leaders to anticipate regulatory shifts, shape external policy, and convert complex data into actionable insights.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Medical Affairs Lead - Lung

This role involves leading the medical input for AstraZeneca's Lung Oncology portfolio, developing and delivering medical plans, and maintaining scientific relationships with key customers. The Medical Affairs Lead will also ensure regulatory compliance and support market access activities, working closely with the Therapy Area Medical Team to drive innovation and excellence.

AstraZeneca London, United Kingdom

Hybrid Permanent

Production / site head - pharmaceuticals

This role involves leading all site operations and radiotracer manufacturing activities, ensuring compliance with UK regulatory requirements. Responsibilities include managing a team of 25, overseeing production processes, maintaining facilities, and contributing to new site development projects. The position is part of a global leader in healthcare technology, offering a collaborative and innovative environment.

Hays Life Sciences London, United Kingdom £65,000 – £80,000 pa

On-site Permanent Clearance Required

Scientific Programme Administrator, Clinical Genomics

The role involves supporting the delivery of high-quality genomics-based External Quality Assessment (EQA) schemes, working closely with scientific and operational teams to ensure accurate and reliable genetic test results. Responsibilities include sample preparation, data handling, quality management, and laboratory support, contributing to international standards in diagnostic genomics.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £32,442 pa

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also supports site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing sophisticated medical and laboratory diagnostic systems used in pathology departments and NHS laboratories. You will visit customer sites, troubleshoot issues, and liaise with laboratory managers and technicians. Full product training is provided.

TRS Consulting Crawley, West Sussex, United Kingdom £45,000 – £48,000 pa

On-site Permanent

QA Officer, Pharmaceutical

The QA Officer will work in a biotech company, focusing on generating and reviewing SOPs, handling customer complaints, and maintaining GMP compliance. They will also participate in quality improvement initiatives, manage documentation, and support regulatory audits.

NMS Recruit Ltd t/a Russell Taylor Group Alderley Edge, Cheshire, SK10 4UB, United Kingdom £28,000 – £34,000 pa

Pharmaceutical/Healthcare Sustainability Lead

We are partnering with a leading organisation in the Pharmaceutical, Healthcare and Retail Eye Care market, to recruit an impactful Pharmaceutical/Healthcare Sustainability Lead who will shape and drive the company’s environmental strategy. In this role, you’ll work closely with senior...

Evolve Selection Birmingham, West Midlands (county), United Kingdom £55,000 – £60,000 pa

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer United States

On-site Permanent