Jobs in Cambridge

Senior Research Scientist – Protein Scientist

The role involves hands-on work in protein biochemistry, including expressing, purifying, and characterizing antibodies and protein constructs. The successful candidate will also perform bioconjugate generation, analytical QC, and collaborate with cross-functional teams to optimize conjugation workflows and evaluate conjugates.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director Integrated Bioanalysis – Biopharma Bioanalytical Program Lead

This role involves leading the bioanalytical strategy for diverse therapeutic modalities, collaborating with global project teams to develop robust assays, and translating complex data into clear program decisions. The position is highly visible, requiring cross-functional influence and external representation of scientific findings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £42,000 – £46,000 pa

On-site Permanent

Post-Doc Engineer - Technical Sales

Post-Doc Engineer - Technical SalesNewton Colmore is working with a technology company in Cambridge, assisting them in their search for the next generation of technical sales and business development talent.This role is perfect for someone who has either just finished...

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.

GSK £242,250 pa

On-site Permanent

Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive successful collaborations and strategic alliances.

GSK £242,250 – £403,750 pa

On-site 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 advanced analytics, AI, and emerging technologies to drive value and impact across Pfizer’s medical portfolio.

Pfizer Test Valley, SO51 6HA, United Kingdom

Remote 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 advanced analytics, AI, and emerging technologies to drive value and impact across Pfizer’s medical portfolio.

Pfizer United States

On-site 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 cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 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 cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

AI Acceleration Lead

This role focuses on driving AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. The person will work across clinical operations, technology teams, and vendors to validate AI tools, generate evidence of value, and guide investment decisions. Emphasis is placed on hands-on testing, change management, and enterprise-wide adoption of AI-native capabilities.

GSK Stevenage, United Kingdom

On-site Permanent

AI Acceleration Lead

Lead the design and execution of AI pilots to solve operational challenges in clinical development, working across clinical operations, technology teams, and vendors. Drive evidence-based scaling of AI solutions, validate feasibility using AI-native tools, and translate findings into strategic recommendations for enterprise adoption.

GSK United States

On-site Permanent