Jobs in Exeter

Senior SME - MSAT EM Tech Ops 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, providing lifecycle support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement and managing technical transfers between contract manufacturing organizations (CMOs).

GSK East Hertfordshire, United Kingdom

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing external partnerships, and ensuring scientific quality and compliance.

GSK Switzerland

Hybrid Permanent

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

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

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-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 submissions and product approvals globally.

Pfizer

On-site Permanent

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

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

Senior Scientist New Modalities, Analytical

This role involves defining and delivering analytical strategies for new modality medicines, such as peptides and oligonucleotides, from early development to commercial launch. You will work closely with cross-functional teams to ensure robust quality control, regulatory compliance, and efficient commercial supply, while leveraging digital tools and AI to enhance decision-making and process robustness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

VP & Global Head, Discovery Chemistry and DMPK, Oncology Targeted Delivery

This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites in Cambridge (UK), Cambridge (MA), and Gaithersburg (US).

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Clinical Trial Manager

The Senior Clinical Trial Manager will manage the execution of clinical trials from start to closure, working closely with the Clinical Project Manager and cross-functional teams. Responsibilities include tracking trial activities, building relationships with CROs, and identifying process improvements. The role is crucial for advancing Recursion's drug development portfolio and ensuring operational excellence across clinical programs.

Recursion United Kingdom £136,200 – £192,200 pa

Hybrid Permanent

Research Associate, Compound Management

The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.

Recursion United Kingdom

On-site Permanent

Senior Manager - Engineering & Maintenance

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

Research Fellow, Translational Vaccine immunology (Tooting)

This role involves designing and delivering pre-clinical and translational immunology studies, including in-vivo murine disease models and ex vivo human immune analyses. The position is part of a dynamic academic environment focused on neonatal infections and maternal-neonatal vaccine responses.

City St George's, University of London (Tooting) London, Tooting, London, SW17 0TF, United Kingdom £51 – £53 pa

On-site Permanent

Research Assistant/Senior Technician, Translational Vaccine immunology (Tooting)

The role involves contributing to a growing programme of translational vaccine research, focusing on neonatal infections and maternal-neonatal vaccine responses. Responsibilities include assay development, quality control, and maintaining high standards of laboratory compliance.

City St George's, University of London (Tooting) London, Tooting, London, SW17 0TF, United Kingdom £34 – £36 pa

On-site Permanent

Principal Scientific Programme Manager, Clinical Genomics

The Principal Scientific Programme Manager will lead and support the delivery of specialist External Quality Assessment (EQA) schemes in clinical genomics. This role involves managing timelines, quality, and programme performance, as well as supporting the design and development of new EQA schemes. The position requires strong scientific knowledge, experience in genomics and quality assurance, and the ability to communicate effectively with senior stakeholders.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £59,157 pa

Hybrid Permanent

Scientific Programme Manager, Clinical Genomics

The Scientific Programme Manager will play a crucial role in international genomics quality assurance, ensuring diagnostic laboratories worldwide produce accurate and reliable genetic test results. Responsibilities include managing EQA schemes, interpreting complex genomic data, and collaborating with senior scientific leaders and stakeholders to maintain high standards and improve diagnostic genomics practices.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £50,169 pa

Hybrid Permanent