Latest Environmental Risk Assessment Scientist 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

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Scientific Expert (CSE) I

Salary Range:£37,593.50 - £69,816.50Job Description SummaryWork Arrangement: Hybrid Working, #LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.ABOUT THE ROLEThe Clinical Scientific...

Novartis London, United Kingdom

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic decisions, optimize investment, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. The Executive Director will lead the creation of comprehensive therapeutic area strategies, provide strategic recommendations to senior leadership, and collaborate across functions to drive innovation and impact.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

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

Mechanical Engineer - Genomics Instrumentation - Cambridge

You will work within a multidisciplinary team to design and develop cutting-edge genomics instrumentation, contributing to high-throughput genomic workflows and precision diagnostics. Your role involves the full product lifecycle, from concept development to product launch.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Biomedical Equipment Engineer / Instrument Technician

This role involves hands-on work assembling, maintaining, and testing a specialist diagnostic instrument. You'll diagnose faults, replace components, and support the product's commercial launch in a laboratory and R&D environment, working closely with the development team.

HCL International Stevenage, Hertfordshire, United Kingdom £30,000 – £40,000 pa

On-site Permanent Flexible

Senior Design Engineer - Medical Devices

The Senior Design Engineer will develop and iterate on a novel surgical visualisation platform, from early-stage concepts to fully-fledged devices. Responsibilities include hands-on prototyping, testing, and documentation, as well as contributing to the R&D strategy and intellectual property management. The role offers significant growth potential and the chance to work in a dynamic, innovative start-up environment.

ETS Technical Beeston, Nottinghamshire, Nottinghamshire, United Kingdom £60,000 – £65,000 pa

Hybrid Permanent

Field Service Engineer

This role involves servicing and maintaining electro-mechanical medical devices in various healthcare settings within the Watford, Enfield, Barnet, and surrounding areas. You will be responsible for fault-finding, equipment maintenance, and providing customer service, with full product training provided.

Redshore Watford, Hertfordshire, United Kingdom £42,000 – £45,000 pa

On-site Permanent

Field Service Engineer

The Field Service Engineer will be responsible for servicing, maintaining, and troubleshooting electro-mechanical medical devices across East and North London. The role involves hands-on work in medical environments, providing customer service and ensuring equipment reliability.

Redshore London, United Kingdom £40,000 – £45,000 pa

On-site Permanent