Biotechnology Jobs

• London
• Hybrid · 2–3 days in office
• Senior

Sits within GSK's Chemical Manufacturing & Control function, shaping how AI transforms manufacturing sites worldwide. Runs day-to-day tech transfer engagement with sites and CMOs, sizes AI opportunities, defines target process, data and agent architecture, and drives agentification and recipe building for new products alongside forward deployed engineering pods.

MES · LIMS · ERP +6

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Sits within GSK's Chemical Manufacturing & Control function, running day-to-day tech transfer engagement with manufacturing sites and CMOs while redesigning processes in detail. Shapes NPI launch strategy covering site impact assessment, capacity management, digital twins, scenario planning and virtual line commissioning, and defines the target process, data and agent architecture. Owns the tech transfer package and drives agentification and MES-ready recipe building alongside forward deployed engineering pods.

MES · LIMS · ERP +6

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• Reading
• Remote
• Mid-level
• Permanent

Oversees vendor activities across global clinical trials from study start-up through close-out, managing central lab, eCOA, IRT, ECG, imaging and patient recruitment vendors. Tracks vendor performance, KPIs and KQIs, drives site readiness and activation, and handles risk mapping, contingency planning and cost control. Home-based within Europe, working in a single-sponsor department.

eCOA · IRT · ECG +1

• Opfikon, Switzerland
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence, and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs. Sits on the Therapy Area Leadership Team, co-leads New Product Opportunity reviews, engages external KOLs and investigators, and drives cross-functional due diligence with BD to close deals.

• Newcastle upon Tyne
• £48,337 – £68,817 pa
• Senior
• Contract

Lead an independent research programme in transplant immunology, focusing on kidney transplantation injury and new therapies, while collaborating with nine senior investigators and the NIHR Blood and Transplant Research Unit. Contribute 0.2 WTE to undergraduate and postgraduate teaching and PhD supervision within the Translational and Clinical Research Institute.

Transplant Biobank

• Coventry
• On-site
• £36,320 – £46,970 pa
• Entry level
• Contract

Postdoctoral role in the Clostridial Cell Biology Group, leading molecular biology and experimental evolution work on vancomycin resistance in Clostridioides difficile. Collaborates with biochemists, bioinformaticians and clinical microbiologists across Warwick, Sheffield, Manchester and Leeds, and involves supervising PhD and masters students.

• London
• On-site
• £27,500 – £30,000 pa
• Entry level
• Temporary

Processing blood and other biofluids from volunteer donors in a research services lab, including centrifugation, buffy coat and PBMC separation, reagent preparation and microbiological/viral testing of urine. Work follows Human Tissue Act, ISO 9001 and internal safety standards, with responsibility for maintaining laboratory records. Suited to someone starting out who has some blood or accredited lab experience.

• United Kingdom
• Remote
• Director · manages people

Senior medical leadership role within a clinical research organisation, acting as a cardiovascular subject matter expert supporting proposals, bid defences and client engagement. Responsibilities span RFP input, protocol and regulatory strategy, internal therapeutic training, and mentoring clinical scientists, with peer-level interaction with pharma medical leadership.

PPD

• Sheffield
• £39,560 – £41,885 pa
• Entry level
• Contract

Contribute to a research programme analysing explanted polymeric medical devices, investigating how implant degradation, tissue responses and patient-specific factors drive complications. Establish experimental and sample-handling workflows, develop lab methods to characterise tissue and immune responses, and collaborate with academic, clinical, regulatory and patient partners including Sheffield Teaching Hospitals and Cambridge.

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• Church Stretton
• Senior

Technical lead role driving innovation in polymeric and silica particle technologies for chromatography, diagnostics and biopharma consumables. Involves independently designing and executing complex polymer synthesis, particle manufacture and surface functionalization, plus technology transfer from lab-scale prototypes to full production. Acts as internal consultant and escalation point for critical materials issues, mentors scientists and shapes long-term technology strategy.

• London
• Hybrid
• Director

Lead global regulatory strategy for renal therapy programs across all development phases, serving as the regulatory representative on cross-functional teams. Drive major submissions such as INDs, NDAs, BLAs and MAAs, and lead health authority interactions, while mentoring regulatory team members. Distinct for its international scope and focus on renal, nephrology and rare disease assets.

IND · CTA · NDA +2

• Cambridge
• Hybrid · 2 days in office
• £65,000 – £80,000 pa
• Senior
• Permanent

Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.

FDA · MHRA · UKCA +2