Biotechnology Jobs in Milton Keynes

Protein Engineering and Innovation Scientist

This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Biomedical Scientist (BMS)

The Biomedical Scientist (BMS) role involves performing analytical testing, operating and maintaining laboratory equipment, and processing patient samples in Blood Sciences disciplines. Responsibilities include result authorisation, quality assurance, and supporting patient care through collaboration with clinical and laboratory teams.

Acorn by Synergie Milton Keynes, Buckinghamshire, United Kingdom £16 – £20 ph

On-site Temporary Shift-work

Director, QC Systems

This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.

GSK Stevenage, United Kingdom

Hybrid Permanent

Research Technician - Life Sciences, Biotechnology

The Research Technician role involves developing and evaluating next-gen chromatography media, supporting method optimisation experiments, and performing analytical testing for membrane chromatography products. The position is part of the Fibro R&D department and focuses on monoclonal antibody purification workflows.

Experis Stevenage, Hertfordshire, United Kingdom £16 ph

On-site Contract

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna Oxford, United Kingdom

On-site Contract

Clinical Trials Associate

The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensuring compliance and inspection readiness. Responsibilities include coordinating documentation, supporting study start-up and close-out, and assisting with site visits and data management.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Patient Safety Partner

The Patient Safety Partner will support individual case safety reports, assess pharmacovigilance requirements, and manage local safety risks within ophthalmology. They will also assist with global safety solutions, product launches, and cross-functional collaboration with Medical Affairs and Clinical Operations.

Talentmark Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £50 – £66 ph

Hybrid Contract

Supplier Quality Engineer - Medical Devices - Oxford

The Supplier Quality Engineer will manage and develop the supplier base for a rapidly growing medical devices company, ensuring compliance with ISO 13485 standards. Responsibilities include evaluating suppliers, managing CAPAs, and applying quality expertise to design-for-manufacture considerations.

Newton Colmore Oxford, Oxfordshire, United Kingdom

On-site Permanent