Biotechnology Jobs in Milton Keynes

Open roles

Salary range

£28k – £516k

Hiring companies

View 72 live roles → Get an alert

Salary on the board

£28k – £516k

Based on advertised midpoints across the 10 priced listings posted in the last 12 months. Base salary only.

By seniority

£k base

Entry

1 job

Junior

1 job

Mid

2 jobs

Senior

150

1 job

Lead

1 job

Director

154

516

4 jobs

Live jobs

72 live roles

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Principal Programmer / Analyst

The Principal Programmer / Analyst role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering innovation and quality assurance in a global, agile environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

(Fixed Term) Manufacturing Associate I

The Manufacturing Associate will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. Responsibilities include maintaining documentation, troubleshooting equipment, and participating in continuous improvement projects in a fast-paced, team-oriented environment.

Moderna Oxford, United Kingdom

On-site Temporary

Fixed Term Manufacturing Associate II

This role involves operating production equipment for mRNA vaccines, adhering to cGMP and safety regulations, and participating in continuous improvement initiatives. The candidate will work closely with QA teams, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, technologically advanced environment.

Moderna Oxford, United Kingdom

On-site Temporary

Safety Process Director / Senior Safety Process Director

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

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