Latest regulatory affairs Jobs

Senior CMC Regulatory Strategy Manager

Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.

Novartis London, United Kingdom

Hybrid Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global teams to ensure patient-centered, evidence-driven medical impact. The role requires deep oncology expertise and strong leadership to influence strategic decisions and communicate scientific data effectively across regions.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions and high-quality medical execution across regions. The position requires deep oncology clinical and scientific expertise, strategic leadership, and collaboration with various stakeholders to deliver impactful medical outcomes globally.

Pfizer

On-site Permanent

Director Biostatistics - Hematology

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...

CSL

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes data integrity, cross-functional collaboration, and integration of emerging technologies, including AI-enabled data analysis, to accelerate clinical development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

This role involves hands-on development, qualification, and validation of functional immunoassays to support mRNA-based clinical trials. The scientist will conduct experiments, analyze data, and ensure regulatory compliance in a GCP environment, contributing directly to patient-impacting therapeutics across multiple disease areas.

Moderna Oxford, United Kingdom

Hybrid Permanent

Design Engineer (Medical Devices / SolidWorks)

This role involves designing and developing medical devices from concept to design freeze, using SolidWorks to create detailed 3D models and drawings. The engineer will collaborate with manufacturing, testing, and project teams to ensure designs meet regulatory and performance standards within a structured development process. The position focuses on creating innovative healthcare products that improve young lives globally.

Ernest Gordon Recruitment Lisburn, County Antrim, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Operations Manager

Role: Operations ManagerSalary: £50,000-£55,000Location: NottinghamshireThe role:We are looking for an experienced Operations Manager to take responsibility for the day-to-day running of a GMP-regulated manufacturing and distribution facility.Reporting into the UK Managing Director, you will have overall responsibility for site operations,...

SKC Recruitment Chilwell, Nottinghamshire, NG9 5FZ, United Kingdom £50,000 – £55,000 pa

Head of Product Development & Engineering

This role involves leading the product development and engineering lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, mentoring a specialist team, and collaborating with quality, operations, and commercial teams to ensure regulatory compliance and commercial success.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent