Biotechnology Jobs

Associate Director, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

Director of Clinical Pharmacology Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic and pharmacodynamic principles to support drug development from early stages through registration and lifecycle management. Develop population PK/PD and exposure-response models, guide dose selection, and present evidence to regulatory bodies. Work within cross-functional teams while maintaining hands-on involvement in quantitative analysis and strategic decision-making.

GSK Stevenage, United Kingdom £183,150 – £305,250 pa

Director of Clinical Pharmacology Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic/pharmacodynamic and exposure-response modelling to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, with a strong emphasis on hands-on quantitative analysis and scientific leadership within a cross-functional environment.

GSK Canterbury, United Kingdom US$183,150 – US$305,250 pa

Associate Director, Clinical Program Management, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and managing timelines, budgets, and vendor partnerships. The role leverages AI and emerging technologies to drive efficient clinical development with a focus on high-probability outcomes. It involves strategic oversight of CROs and collaborators while ensuring alignment between clinical objectives and company goals.

Isomorphic Labs England

Hybrid Permanent

General Application - Register Your Interest

This is a general interest application for roles at Isomorphic Labs, an AI-driven drug discovery company. Candidates may be considered for positions including Software Engineers, ML Researchers, Computational Chemists, and Technical Project Managers. The role involves interdisciplinary collaboration to advance AI models for rational drug design and digital biology, within a culture emphasising curiosity, bravery, determination, and teamwork.

Isomorphic Labs United Kingdom

Hybrid Permanent

Laboratory Technician - Plant Cell Culture

This role involves hands-on support for plant tissue and cell culture experiments within a cutting-edge research environment focused on sustainable agriculture and food production. The technician will prepare media, maintain cultures, monitor growth and contamination, and ensure aseptic conditions, contributing to scalable plant-based solutions. Close collaboration with researchers and automation specialists supports reproducible, high-quality scientific workflows in a state-of-the-art lab setting.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Media and Glass Technician - Generative Biology Institute

This role involves preparing laboratory media, buffers, and agar plates while maintaining sterile glassware and consumables to support high-quality research at the Generative Biology Institute. The technician ensures consistent, contamination-free supplies using aseptic techniques and standard operating procedures, enabling scientists to focus on engineering biology breakthroughs. The position emphasizes precision, routine quality control, equipment operation, and collaboration within a dedicated support team in a state-of-the-art research environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Director, International HEOR & HTA, Immunology

This role involves developing and executing HEOR and HTA strategies for Novartis' Immunology portfolio, ensuring payer and HTA evidence requirements are integrated into clinical development plans. You will partner with various teams to maximize asset value and translate complex evidence into compelling value stories for healthcare decision-makers.

Novartis London, United Kingdom

Graduate Pharmaceutical Quality Technician

This role involves conducting final quality checks on aseptically prepared medicines, ensuring compliance with SOPs and GMP standards. You will work closely with QA Releasers and Production Pharmacists, using automated equipment and confirming product quality before release.

ITH Pharma Middlesex, London, United Kingdom £30,073 pa

Pharmaceutical Checking Technician

This role involves checking aseptically prepared medicines against approved procedures, completing in-process checks, verifying documentation, and reconciling raw materials. The position offers structured training, a clear salary increase, and the opportunity to work in a regulated pharmaceutical environment.

ITH Pharma Middlesex, London, United Kingdom £27,618 pa

Study Start-Up Team Lead

The Study Start-Up Team Lead at Novartis will guide a team in the activation of clinical trials, ensuring operational excellence and compliance. Key responsibilities include driving innovative practices, collaborating with cross-functional teams, and maintaining inspection readiness.

Novartis London, United Kingdom £67,900 – £126,100 pa

Higher Scientific Officer Postdoctoral Scientist - Molecular Virology

Conduct molecular virology research within a government biosciences institute, focusing on laboratory-based analysis and scientific reporting. Work is primarily based in Belfast with potential for multi-site collaboration across Northern Ireland. The role supports statutory and scientific objectives in animal and plant health.

Agri-Food and Biosciences Institute (AFBI) Belfast, Northern Ireland, United Kingdom £37 – £38 pa

Permanent

Head of Quality, Pharmaceutical

Lead the quality function in a GMP-regulated pharmaceutical manufacturing environment, overseeing QA, QC, and compliance systems. Drive quality strategy, regulatory readiness, and continuous improvement across operations. Manage audits, inspections, and a high-performing team within a growing organisation.

NMS Recruit Ltd t/a Russell Taylor Group Boothstown, Manchester, M28 1LT, United Kingdom £60,000 – £65,000 pa

On-site Permanent

GCP Quality Manager (12

The Quality Manager role involves providing quality oversight across clinical activities and the Quality Management System (QMS). Responsibilities include leading and supporting audits, managing quality events, and contributing to regulatory inspection readiness. The role requires significant QA experience in the pharmaceutical or clinical research sectors, strong knowledge of GCP, GCLP, and GPvP, and experience with quality management systems and regulatory inspections.

HAYS Specialist Recruitment Ox13Pa, United Kingdom

Contract