Jobs in Exeter

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

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation priorities into portfolio planning. The position requires deep clinical expertise and a proven track record in business development and deal-making.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and site selection criteria. The role also involves training and supporting site-facing colleagues, participating in safety review meetings, and contributing to continuous improvement initiatives.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 supporting site selection, training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a pharmaceutical manufacturing environment, ensuring compliance with GMP regulations. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Quality Engineer

The Quality Engineer will manage product quality issues, implement corrective actions, and collaborate with cross-functional teams to enhance quality and optimize processes. Key responsibilities include leading problem-solving sessions, monitoring quality metrics, and supporting new product introductions.

Azenta Life Sciences Wotton, Surrey, Surrey, United Kingdom

On-site Permanent

QA Officer, Pharmaceutical/Biotech

QA Officer, Pharmaceutical/BiotechLocation: Cheshire (onsite)Type: PermanentSalary: £28,000-£33000 (dependant on experience)Hours: Days (Monday - Friday), parking onsiteAdditional: 25 days holiday + BH, private medical, share options scheme, company pensionOur Client a Biotech company is looking to strengthen their QA team and...

NMS Recruit Ltd t/a Russell Taylor Group Wilmslow, Cheshire, United Kingdom £28,000 – £33,000 pa

Quality Assurance Officer

The Quality Assurance Officer will manage ISO 9001 activities, maintain QMS documentation, oversee training records, and conduct internal and external audits. This hands-on, site-based role is crucial for ensuring compliance and audit readiness in a growing biotechnology company focused on high-quality product development.

Reed Cb58Hw, CB5 8HW, United Kingdom £35,000 – £40,000 pa

On-site Permanent

Senior Scientist or Associate Principal Scientist Metabolist Team

This role involves conducting advanced in vitro and ex vivo research to identify and validate therapeutic targets for obesity. The successful candidate will work in a dynamic, collaborative environment, designing and implementing experiments, analyzing data, and contributing to drug discovery projects across multiple sites.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible