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On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

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AstraZeneca

Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

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Moderna

Oxford, United Kingdom

Hybrid Permanent

Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech...

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CSL

On-site Permanent

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 role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

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GSK

East Hertfordshire, United Kingdom

Hybrid Permanent Flexible

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

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Autolus

Stevenage, United Kingdom

On-site Permanent

Software Engineer (Data Services), London

This role involves working in a fast-paced, interdisciplinary team to build a cutting-edge ML-based software platform for drug discovery. Responsibilities include data engineering, service-oriented architecture, and collaboration with scientists and ML researchers to accelerate scientific breakthroughs.

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Isomorphic Labs

London, United Kingdom

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Where to Advertise Biotech Jobs in the UK (2026 Guide)

Where to advertise biotech jobs UK in 2026: the specialist boards, academic networks and trade channels that reach biotech R&D and bioprocessing talent. The candidate pool spans life scientists, computational biologists, regulatory specialists and biomanufacturing engineers — each with distinct professional networks and job search behaviours. General job boards reach a broad audience but lack the specificity that biotech professionals expect. Specialist platforms, academic channels and sector-specific communities each serve a different part of the market. This guide, published by BiotechnologyJobs.co.uk, covers where to advertise biotech roles in the UK in 2026, how the main platforms compare, what employers should expect to pay, and what the data says about hiring across different role types.

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