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

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, 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

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

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

Postdoctoral Research Associate in Molecular Evolution and Functional Genomics (Fixed Term)

The role involves conducting interdisciplinary research at the intersection of molecular evolution, functional genomics, and machine learning. The postholder will manage their own research, contribute to graduate student development, and collaborate with researchers in computational biology, genetics, and applied mathematics.

University of Cambridge Cambridge, South East England, United Kingdom £37 – £46 pa

On-site Contract

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

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Research Investigator, (Biologics Pharmacology), London

As a Senior Research Investigator, you will contribute to the pharmacology and translational biology strategy of novel large molecule therapeutics, leveraging Isomorphic Labs' cutting-edge AI drug design engine. You will design and execute pharmacology plans, lead in vivo and in vitro evaluations, and collaborate with interdisciplinary teams to advance drug discovery projects from early stages to clinical candidates.

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