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 to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK

Hybrid Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

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. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

On-site Permanent

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom

Hybrid Permanent

Senior Technical Program Manager (Preclinical), London

This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.

Isomorphic Labs London, United Kingdom

On-site Permanent

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom

Hybrid Permanent

Disease Level Partner - South Central UK

The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.

Roche United Kingdom

On-site Permanent

Associate Director, Resilience Strategic Partnerships – UK

This role involves leading the execution of Moderna's strategic partnership with the UK government, focusing on mRNA-based vaccines and biomanufacturing. You will manage day-to-day interactions with key government stakeholders, represent Moderna on the UKHSA operations board, and drive cross-functional collaboration to deliver public health impact.

Moderna Tameside, SK15 3JG, United Kingdom

On-site Permanent

Synthetic Chemistry Lead, London

As a Synthetic Chemistry Lead, you will apply your expertise to drive medicinal chemistry and CMC projects, collaborating with multidisciplinary teams and external partners. You will play a key role in advancing drug discovery programs and representing the company to collaborators, while fostering a culture of inclusion and continuous development.

Isomorphic Labs United Kingdom

Hybrid Permanent

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

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 Oxford, United Kingdom