Biotechnology Jobs

• Stevenage
• Hybrid
• Senior

Hands-on senior role owning the computerised-system lifecycle for GxP systems, from impact and supplier assessments through validation, release, operation and retirement. Authors and executes CSV documentation, performs data integrity and 21 CFR Part 11 assessments, manages change controls and CAPAs, and supports regulatory inspections as a CSV subject matter expert.

SaaS · Cloud

• Oxford
• On-site
• Mid-level

Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.

Emerson DeltaV · Allen-Bradley · Rockwell Automation +7

• Oxford
• On-site
• Senior

Hands-on maintenance of GMP manufacturing equipment at a new mRNA vaccine facility, including autoclaves, filling lines, isolators, TFF systems and chromatography skids. Acts as first responder to equipment failures, performing structured root-cause troubleshooting, preventative maintenance, CAPA work and cGMP documentation, while coordinating vendors and contractors. Includes on-call rotation for 24/7 operations and OJT delivery.

Excel · Word · PowerPoint +1

• London
• On-site
• Director

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.

Generative AI

• Abingdon
• Director · manages people
• Permanent

Leads Evotec's consolidated AI Accelerator, owning machine learning, generative and agentic AI, and therapeutic hypothesis groups. Sets the AI vision and roadmap, makes build/buy/partner decisions for the AI stack, and turns proprietary multi-omics and experimental data into predictive models and reusable IP. Acts as the senior external technical voice for AI in drug discovery.

• London
• Hybrid
• Mid-level
• Permanent

Join the Platform Team to design and scale Kubernetes-based hybrid compute clusters across private and public clouds, building core platform services and APIs. You will enhance CI/CD pipelines, monitoring, backup and disaster recovery, while partnering closely with Machine Learning and Data Science teams to support their computational needs.

Kubernetes · GitHub Actions · ArgoCD +3

• Wrexham
• Director · manages people

Leads Ipsen's global Biologics Process Development organisation, owning CMC drug substance strategy for toxins, monoclonal antibodies, ADCs and enzymes from candidate selection through launch and lifecycle. Manages process and analytical development teams, acts as CMC sponsor, and directs CDMO partnerships, tech transfer and regulatory submissions. Also serves as PharmDev/R&D site lead in Wrexham on the cross-divisional Site Leadership Team.

CDMOs

• London
• Hybrid
• Mid-level

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.

RIMS

• London
• Hybrid · 3–4 days in office
• Senior

Shapes and executes a UK-wide government affairs strategy as a sole contributor, focusing on respiratory vaccines and building relationships across government, Parliament and industry. Involves legislative and regulatory analysis, trade association management, and exploring Generative AI for policy intelligence, working with Communications, Medical and Market Access teams.

Generative AI

• Oxford
• On-site
• Senior

Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.

Grants Manager · GrantPlan · MS Office +1

• London
• Hybrid
• Director · manages people

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Microsoft Office