Latest regulatory affairs Jobs

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and improving processes.

GSK United States

Hybrid Permanent

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and contributing to process improvements.

GSK

Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves developing and maintaining global labelling strategies and core documents for oncology products, ensuring compliance and consistency across different markets. You will lead cross-functional discussions, present proposals to governance bodies, and mentor colleagues while staying updated on regulatory changes and competitor activities.

Novartis London, United Kingdom

Hybrid 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

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate high-quality medical insights. Key responsibilities include developing strategies, prioritizing use cases, and applying advanced analytics and AI to inform medical decision-making. The role also focuses on embedding insights into core medical processes and collaborating with various stakeholders to ensure effective use of insights.

Pfizer

On-site Permanent

Senior Counsel

The Senior Counsel provides comprehensive legal support and advice to AstraZeneca's UK marketing company, focusing on AI, data privacy, and commercial matters. They will act as a subject matter expert, draft and review legal documents, and ensure compliance with regulations and internal policies.

AstraZeneca London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global regulatory CMC strategy and submissions for mRNA-based medicines, ensuring compliance with international regulations. Guide cross-functional teams on regulatory requirements and oversee documentation for biologics across vaccine, oncology, and rare disease programs. Drive process improvements and interact directly with health authorities to support product development.

Moderna London, United Kingdom

Hybrid Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

On-site Permanent

Technical Documentation and Development Engineer

This role involves creating, managing, and improving technical documentation and CAD models for medical devices, ensuring compliance with MDR regulations. The engineer will own technical files, support product development and legacy improvements, and collaborate with R&D, regulatory, and manufacturing teams. Emphasis is placed on accuracy, regulatory adherence, and structured design control processes.

Michael Page Sheffield, South Yorkshire, United Kingdom £42,000 pa

On-site Permanent

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

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

Vice President, Head of Strategy & Operations

Your work will change lives. Including your own.The Impact You'll MakeRecursion is reimagining drug discovery through the integration of automated cell biology, high-dimensional data, and AI-driven analytics. As Head of Strategy & Operations, you will be our CEO's closest strategic...

Recursion North Tyneside, NE29 8EP, United Kingdom