Latest Pharmaceuticals Jobs

Vice President, Medical Affairs

The Vice President, Medical Affairs, will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare disease, and immunology. Key responsibilities include building evidence-generation plans, engaging with key opinion leaders, and ensuring compliance with medical and regulatory standards.

Recursion United Kingdom

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This is a general talent network sign-up opportunity rather than a specific job role. Candidates can submit their resume for future consideration at Recursion, a clinical-stage TechBio company using AI and automated biology to accelerate drug discovery. The company emphasizes bold, ethical innovation and cross-functional collaboration to address unmet medical needs.

Recursion United Kingdom

On-site Permanent

Design Engineer

This role involves creating detailed mechanical and electro-mechanical designs for industrial machinery, focusing on improvement, modernisation, and refurbishment projects. The engineer will produce schematics, assembly drawings, BOMs, and P&IDs, ensuring compliance with UK and international standards. Work spans process machinery used in sectors like pharmaceuticals, food, and oil & gas, with some international travel required.

ASL Winchester, Hampshire, United Kingdom £40,000 – £55,000 pa

Associate Director, Patient Engagement

This role involves leading patient engagement initiatives in clinical research, ensuring patient perspectives shape clinical trial design, and building relationships with patient advocacy groups and healthcare institutions. The position requires significant experience in clinical research and patient engagement, with a focus on protocol development and site management.

CSL United Kingdom

Hybrid Permanent

Quality Manager (m/f/x) - EU-based

The Quality Manager role involves maintaining and improving quality management systems, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with cross-functional teams, manage quality processes, and implement electronic quality systems.

CSL Italy

Inspection Assembly & Packaging Operations Manager

Lead inspection, assembly, and packaging operations in a regulated pharmaceutical environment, ensuring safety, quality, and on-time delivery. Drive continuous improvement, coach frontline teams, and support new product introductions in collaboration with engineering and quality teams. Operate within a GMP-compliant manufacturing site with a focus on compliance, efficiency, and people development.

GSK Barnard Castle, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.

Moderna London, United Kingdom

On-site Permanent

CMO Planning Integration Manager

This role involves leading the planning integration between contract manufacturing organizations and GSK supply teams in the UK. Responsibilities include building integrated supply plans, identifying and mitigating supply risks, and driving process standardization and continuous improvement.

GSK

Associate Director, Clinical Supply Chain, Cambridge, MA

This role involves leading end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory management, and global distribution. You will work closely with Clinical Operations and the Clinical Development team to ensure seamless clinical trial execution and compliance with regulatory standards.

Isomorphic Labs Cambridge, United Kingdom

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Multi-Skilled Engineer II

The Multi-Skilled Engineer II role involves maintaining and repairing pharmaceutical equipment and facility installations to support manufacturing and QC operations. Responsibilities include diagnosing and repairing equipment, conducting risk assessments, planning maintenance, managing critical spares, and providing support to other teams.

Autolus Stevenage, United Kingdom

Lecturer in Biotechnology and Applied Bioscience

Our MissionPeoplesFuture Ltd (a sister company of Coventry University) provides a sector leading, dedicated inclusive service to Coventry University Group students supporting their successful global education experience and graduate employment outcomes. Tailoring our service to each students’ individual needs and...

Coventry University Group (CUG) Coventry, Midlands Of England, United Kingdom £39 – £44 pa

Permanent

Associate Director, Pipeline Intelligence and Reporting

This role involves managing and enhancing project and pipeline data, reporting, and analytics to support operational and strategic decision-making across Novartis Development. The Associate Director will translate complex data into actionable insights, partner with cross-functional stakeholders, and continuously improve reporting and portfolio outcomes.

Novartis London, United Kingdom

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Global Site and Study Operations Contracting Undergraduate

This role involves hands-on experience in clinical site contracting, including drafting and negotiating contracts with clinical trial sites and investigators. The candidate will work closely with an experienced team lead, gaining insights into legal terms, budget concepts, and regulatory requirements. There are also opportunities to support process improvement and other functions within Global Site and Study Operations (GSSO).

Pfizer Sandwich, United Kingdom