Biotechnology Jobs in Milton Keynes

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

Biologics Account Manager

This role involves driving clinical demand for respiratory biologics by building strategic relationships with healthcare professionals and multi-disciplinary teams across a defined UK territory. The Account Manager will lead formulary access, support homecare utilization, and collaborate with cross-functional teams to implement account plans in complex secondary care environments. Success requires strong commercial acumen, stakeholder influence, and deep understanding of the NHS commissioning landscape.

AstraZeneca Sheffield, United Kingdom

On-site Permanent

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

QC Analytical Scientist

The role involves performing analytical testing in a GMP-compliant laboratory environment, including in-process and release testing of drug products using techniques such as ddPCR, flow cytometry, sterility testing, and endotoxin assays. The scientist ensures data integrity, supports method validation and tech transfer, investigates quality events, and maintains laboratory compliance. This is a shift-based position requiring hands-on work with cell-based therapies in a regulated, cleanroom setting.

Autolus Stevenage, United Kingdom

On-site Permanent Shift-work

Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

Engineering Manager

The Engineering Manager (Shift) leads a multiskilled team responsible for maintaining pharmaceutical equipment and utility systems in a GMP-regulated manufacturing environment. This role involves overseeing reactive and planned maintenance, managing contractors, conducting risk assessments, and ensuring compliance with GDP, ALCOA, and GMP standards. The position operates on rotating shifts and requires strong leadership, problem-solving, and technical expertise in cleanroom operations and controlled systems.

Autolus Stevenage, United Kingdom

Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across markets. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on innovation, patient impact, and strategic decision-making within a matrix environment.

GSK Stevenage, United Kingdom

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in exposure-response analysis, population PK/PD, and quantitative systems pharmacology within a cross-functional R&D environment.

GSK Stevenage, United Kingdom £119,250 – £198,750 pa

Software Engineer - Orchestration

This role involves building the execution engine for autonomous laboratories, bridging AI-driven decision-making with reliable, safe control of laboratory hardware. You'll design systems that translate high-level agent intent into precise, observable, and recoverable sequences of actions, ensuring operations remain within biological and mechanical constraints. The work emphasizes robustness, closed-loop validation through sensors and feedback, and handling failures gracefully in real-world scientific environments.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Microfluidics Engineer

Design and develop microfluidic sample preparation systems for a diagnostic platform that enables rapid bacterial identification and antimicrobial susceptibility testing from whole blood. Work across the full lifecycle from concept to scale-up, conducting prototyping, experimental validation with biological samples, and design for manufacturability within a regulated environment. Collaborate closely with scientists and engineers to optimise fluidic performance and ensure robust, scalable microfluidic cartridges.

Platform Recruitment Oxford, Oxfordshire, United Kingdom £50,000 – £75,000 pa

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