Jobs in Cambridge

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory expertise to guide product development across medical and non-medical technologies, ensuring compliance with international standards such as ISO 13485, FDA 21 CFR 820, and ISO 9001. The specialist will work embedded within project teams, interpreting evolving regulations, supporting quality systems, and enabling innovation while maintaining regulatory alignment throughout the product lifecycle.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Head of Global Regulatory Affairs and Strategy, Cambridge, MA

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

Medical Director, Clinical Development (Oncology), Cambridge, MA

This role involves leading the clinical development of oncology drug candidates derived from AI-driven insights, translating them into actionable trial strategies, and ensuring scientific and regulatory rigor. The Medical Director will act as the primary medical monitor, guide cross-functional teams, and represent the company in interactions with regulators and key opinion leaders. The position emphasizes patient safety, protocol compliance, and strategic input from discovery through clinical proof-of-concept.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Feasibility and Recruitment Lead

This role involves leading UK feasibility and recruitment for cutting-edge cell therapy studies, translating scientific insights into actionable plans. Responsibilities include guiding end-to-end feasibility, collaborating with global stakeholders, and developing recruitment strategies to ensure timely and effective patient access to trials.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Manufacturing Engineer - Medical Technology

This role involves leading manufacturing process development for novel medical sensor technology, transitioning products from development to production. The engineer will drive design for manufacture, conduct process optimization with prototypes, and support design verification through jig and fixture validation. A key focus is ensuring quality and cost-effective manufacturing while shaping team practices in a multidisciplinary, innovation-driven environment.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Commercial Associate Director - Services

The Commercial Associate Director will lead contract negotiations, manage strategic client relationships, and drive proposal and bid management for Nuclera's lab services. Key responsibilities include pricing discussions, managing key accounts, and developing commercial strategies to support market expansion and revenue growth.

Nuclera Cambridge, United Kingdom

Hybrid Permanent

Laboratory Technician - Service Fulfillment

Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. The company’s mission is to improve human health by making proteins accessible. We are beginning this mission through the launch of our eProtein...

Nuclera Cambridge, United Kingdom

On-site Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.

GSK £189,750 – £316,250 pa

On-site Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating these into clinical plans to optimize decision-making and patient stratification.

GSK £189,750 – £316,250 pa

On-site Permanent

Sales Manager (Clinical Diagnostic Services)

This role involves driving new business and expanding customer relationships in the UK health and wellness screening market within clinical diagnostics. The candidate will lead tender processes, develop commercial opportunities, and collaborate with technical teams to deliver tailored solutions. It's ideal for someone with a scientific background looking to transition into a commercial role focused on strategic growth in a science-led environment.

VRS UK Oxford, Oxfordshire, United Kingdom £50,000 – £60,000 pa

Hybrid Permanent

Regulatory Affairs Specialist

The role involves providing technical regulatory support for the international distribution of diagnostic products, ensuring compliance with CE marking and global medical device regulations. Responsibilities include validating product claims, maintaining up-to-date documentation, and reviewing complaints for regulatory reportability. The position is based at the Innovation Centre in Bedford with hybrid working options.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £30,000 – £35,000 pa

Hybrid Contract

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.

Pfizer United States

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will lead the generation of health economics and outcomes research, manage global value dossiers, and coordinate with cross-functional teams to ensure a consistent and robust evidence strategy.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent