Latest regulatory affairs Jobs

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.

GSK

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 improving processes.

GSK United States

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, 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, 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 contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Director, Alliance Management

This role involves leading strategic partnerships with CROs, ensuring governance, performance, and relationship management. The Director will collaborate globally, drive continuous improvement, and support cross-functional teams at AstraZeneca's Cambridge Biomedical Campus.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Research Associate - Technical Development maternity cover

The Research Associate will work closely with the R&D and manufacturing teams to develop and optimize manufacturing processes for CAR-Treg therapies. Responsibilities include conducting experiments, managing databases, improving process design, and handling mammalian and primary human immune cell cultures. The role requires on-site presence and flexibility to travel between London sites.

Quell Therapeutics London, W12 7RH, United Kingdom

On-site Permanent

Associate Director/Director of Statistical Programming

This role involves leading statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, and analysis datasets. You will oversee external vendors, develop standards and innovative technologies, and support data-driven decision-making in drug discovery.

Recursion United Kingdom £200,600 – £260,200 pa

Remote Permanent

Optical Systems Engineer - Medical Devices - Cambridge

This role involves designing and integrating optical systems into complex medical technologies, from early feasibility to product launch. You'll collaborate with a multidisciplinary team to develop devices that improve diagnostics, treatment, and patient outcomes, with a focus on precision, creativity, and regulatory compliance.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Production / site head - pharmaceuticals

This role involves leading all site operations and radiotracer manufacturing activities, ensuring compliance with UK regulatory requirements. Responsibilities include managing a team of 25, overseeing production processes, maintaining facilities, and contributing to new site development projects. The position is part of a global leader in healthcare technology, offering a collaborative and innovative environment.

Hays Life Sciences London, United Kingdom £65,000 – £80,000 pa

On-site Permanent Clearance Required

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Worsley, Manchester, M28 2GE, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Chief Technology Officer

The Chief Technology Officer will lead the technology and product development strategy for a rapidly growing MedTech company. Key responsibilities include guiding multidisciplinary teams, translating customer and commercial requirements into product priorities, and ensuring regulatory compliance. The role involves close collaboration with executive leadership and external stakeholders.

Cure Talent Nottingham, Nottinghamshire, United Kingdom £100,000 – £120,000 pa

On-site Permanent