Jobs in Exeter

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, supporting new product introductions, and managing engineering programs for Large Molecule Drug Substance. The position requires expertise in engineering aspects of large molecule drug substance and involves site assessments, capital management, and troubleshooting.

GSK

On-site Permanent

Specialist - Extractables and Leachable - MSAT EM

This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk escalation for biopharmaceutical manufacturing processes and packaging systems.

GSK £70,650 – £117,750 pa

On-site Permanent

Head of Make CoE

The Head of Make CoE will lead the transformation of end-to-end manufacturing processes across a global network, partnering with sites and central teams to deliver safer, higher-quality, more sustainable, and more productive operations. Key responsibilities include strategy and roadmap leadership, governance, cross-functional integration, and team development, with a focus on digital and autonomous manufacturing.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Senior Director, Head of AI for Clinical Development, Early BPRD

This role involves leading the development and application of AI in early phase clinical trials for AstraZeneca, focusing on Phase I/II programs. You will build and manage a team of AI researchers and engineers, develop reusable AI methods, and collaborate with domain experts to improve clinical trial design and decision-making.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.

Pfizer

Medical Director, Gastroenterology, Early Clinical Development

This role involves leading global clinical trial teams through phase 1 and 2 development, drafting early clinical development plans, and serving as a medical lead for early clinical studies. The Medical Director will collaborate with biomarker experts, research scientists, and key opinion leaders to identify and implement strategies for preclinical and clinical support of gastroenterology programs.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Medical Lead - Respiratory

This role involves leading the medical strategy for GSK's specialty respiratory portfolio, ensuring patient needs are at the forefront. Responsibilities include managing a medical therapy team, developing strategic plans, and engaging with healthcare professionals and regulatory bodies.

GSK United Kingdom

Hybrid Permanent

Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom

On-site Permanent

Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent