Jobs in Exeter

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and repair of advanced medical diagnostic systems in NHS and private laboratories, ensuring minimal downtime through proactive maintenance and technical troubleshooting. Work closely with lab personnel to deliver reliable diagnostic solutions while receiving full product training. Role involves frequent customer visits and some weekend work as part of a five-day working week.

TRS Consulting Stirling, Stirling And Falkirk, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings, including on-site troubleshooting and breakdown response. The engineer will work with high-value, complex equipment and provide technical solutions directly to laboratory staff. Full product training is provided, and the role requires a flexible schedule with some weekend work.

TRS Consulting Portsmouth, Hampshire, United Kingdom £52,000 pa

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

Associate Director, Biostatistics

This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.

CSL

Hybrid Permanent

SERM Scientific Director

Leads safety evaluation and risk management for GSK's oncology assets in clinical development, providing scientific expertise to assess and communicate safety risks globally. Works cross-functionally to shape safety strategy, support regulatory submissions, and ensure patient protection. Focuses on signal detection, risk assessment, and strategic decision-making in a matrix environment.

GSK £111,750 – £186,250 pa

On-site Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays—including RT-qPCR, dPCR, and NGS-based methods—for clinical biomarker programs at Moderna. The scientist will drive end-to-end assay lifecycle management, ensure compliance with GCLP and regulatory standards, and collaborate across multidisciplinary teams to generate high-quality genomic data. A key focus is integrating genomics, bioinformatics, and clinical insights to support drug development and inform future pipeline strategies.

Moderna

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Moderna

Hybrid Permanent

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

Director of Nonclinical Safety, Cambridge, MA

Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.

Isomorphic Labs Cambridge, United Kingdom

Director, Oncology Translational Medicine Project Manager

The Director, Oncology Translational Medicine Project Manager, will lead project management for biomarker and diagnostic strategies across GSK’s global Oncology portfolio. Responsibilities include managing external alliances, regulatory submissions, and diagnostic target profiles, ensuring high-quality data and documentation support oncology asset development and approvals.

GSK Canterbury, United Kingdom £189,750 – £316,250 pa

Scientist, Advanced Genome Technologies - Plant Biology Institute

This role involves designing and conducting experiments in advanced genome technologies and next-generation plant transformation to enhance plant engineering capabilities. The scientist will work on genetic manipulation, DNA/RNA delivery, and plant regeneration, contributing to high-impact research with real-world applications in food security and sustainable agriculture. Collaboration with AI, automation, and generative biology experts across EIT’s ecosystem is a key part of the role.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

AI & Automation Lead for Plant Transformation - Plant Biology Institute

Lead the integration of AI, robotics, and automation in plant transformation workflows to accelerate scalable, data-rich platforms for plant science. Provide subject matter expertise in plant biology while co-developing computer vision systems, predictive ML models, and high-throughput pipelines. Drive project execution, scientific translation, and commercialisation within a multidisciplinary team focused on transforming lab-based discoveries into real-world agricultural and environmental solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Research Assistant in Microbial Genomics

This role involves managing and analysing a large collection of over 60,000 Neisseria gonorrhoeae genomes to study antimicrobial resistance, vaccine antigen diversity, and pathogen evolution. The postholder will develop and apply bioinformatics workflows for genome annotation, conduct population genomic analyses, and contribute to research dissemination through publications and presentations. Work will be conducted within a multidisciplinary team at the University of Oxford, with opportunities to support teaching and mentoring activities.

University of Oxford Oxford, South East England, United Kingdom £35 – £41 pa

Contract

Quality Officer (GDP)

This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance activities such as managing deviations, change controls, audits, and supplier verifications. The Quality Officer will support the Quality Management System, conduct investigations, review documentation, and prepare for regulatory inspections. They will work closely with internal teams and external stakeholders to maintain product quality and process safety in a regulated environment.

Adecco United Kingdom

Hybrid Permanent