Biotechnology Jobs

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The position also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK United States

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing partnerships with academic centers, and ensuring scientific quality and compliance.

GSK

On-site Permanent

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, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, team-oriented environment.

Moderna

On-site Temporary

(Fixed Term) Manufacturing Associate I

The Manufacturing Associate I will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. They will work in a highly technological environment, collaborating with QA teams, troubleshooting issues, and participating in continuous improvement projects.

Moderna

On-site Temporary

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

GMP Vendor Oversight and QA Lead

This role involves leading the quality oversight of external partners in R&D and regulated activities, ensuring compliance with GxP standards. Responsibilities include vendor lifecycle management, risk-based monitoring, quality agreements, and cross-functional collaboration to maintain high-quality standards and continuous improvement.

CSL United Kingdom

On-site Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent

Sr. Data Platform Engineer - Computer System Validator

As a Senior Data Platform Engineer, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will collaborate with biologists, chemists, and data scientists to make Recursion’s vast datasets discoverable and queryable, supporting the company’s mission to advance drug discovery through technology and biology.

Recursion United Kingdom £142,500 – £220,500 pa

Hybrid Permanent

Research Associate - Biology Automation

This role involves developing and running automated biochemical and cell-based assays to support drug discovery projects. You will work on a leading-edge automation platform, ensuring high-quality data and collaborating with cross-functional teams to drive small molecule therapeutics development.

Recursion Crathes, Alba / Scotland, United Kingdom

On-site Permanent

Talent Partner (Tech), London

As a Talent Partner at Isomorphic Labs, you will play a critical role in building world-class teams by developing and executing talent acquisition strategies. You will partner with senior leaders to attract top-tier talent, shape the company's future, foster an inclusive culture, and enhance the employer brand in the competitive AI and biotech landscape.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Product Manager

Senior Product ManagerUK Remote FirstSalary up to £105,000This is a high impact Senior Product Manager role where you will shape and elevate a growing product function at the heart of life sciences innovation. You will own the product direction end...

Harnham - Data & Analytics Recruitment London, United Kingdom £90,000 – £105,000 pa

Permanent

Senior Group Director, Safety Development & Processes

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

Data Scientist (Analytics), London

As a Data Scientist at Isomorphic Labs, you will work with a multidisciplinary team to analyze business intelligence data, implement telemetry, and design key metrics to optimize the drug design process. Your role involves providing actionable insights to drive decision-making across product, engineering, and research teams, and collaborating to build an analytics layer that supports efficient drug discovery.

Isomorphic Labs London, United Kingdom

On-site 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