Biotechnology Jobs

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

Embedded with chemical manufacturing teams, you build in-silico process models, digital twins and optimization solutions, taking proofs of concept to deployed MVPs at a days-to-weeks cadence. Work is AI-augmented, with coding agents handling routine development while you focus on model identification, scenario planning and handing proven solutions to solutions engineers.

Claude Code · GitHub Copilot · Databricks AI Assistant +4

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

Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• 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

• London

Act as a self-employed field sales agent promoting point-of-care diagnostic solutions to healthcare providers including care homes, pharmacies, and GP practices. Leverage existing relationships to sell diagnostic devices and reagent cartridges, supported by full training and biomedical expertise. Generate income through upfront and recurring commissions from consumable sales.

• Oxford
• £50,000 – £65,000 pa
• Lead

Hands-on lab role owning assay design, development and delivery across plant biology and cell science. Involves building mode-of-action assays, developing automated high-throughput analysis pipelines, and sharing plant physiology expertise across multidisciplinary teams while mentoring colleagues on experimental records and protocols.

Brightfield Microscopy · Fluorescence Microscopy

• Oxford
• On-site
• Lead
• Permanent

Leads vector design strategy for gene edited and transgenic crop programmes, covering expression cassette architecture, guide RNA modules, donor templates and multiplex editing configurations. Owns the design-to-vector-release process, including construct QC, sequence management, vendor workflows and handover packages for transformation teams. Builds an industrial-grade vector design capability for corn, wheat and other strategic species, with SOPs, LIMS/ELN tracking and mentoring of scientists.

ELN · LIMS

• Oxford
• On-site
• Mid-level · manages people
• Permanent

Leads the end-to-end event delivery workflow for gene edited and transgenic crops, from transformation output through sampling, molecular confirmation, QC review and handover. Designs and validates genotyping assays (PCR, qPCR, ddPCR, KASP, NGS) and builds stage-gate criteria, LIMS-enabled tracking and vendor strategies across corn and wheat programmes.

Endpoint PCR · qPCR · ddPCR +6

• Cambridge
• On-site
• Senior
• Permanent

Formulate, dispense and quality-control reagents for a protein discovery platform, operating lab equipment such as pipettes, centrifuges and UPLC systems. The role covers batch documentation, inventory management via ERP and troubleshooting production deviations, working closely with R&D, QA and Supply Chain in a fast-paced lab environment.

UPLC · ERP

• Stevenage
• Remote

Serves as the primary point of contact for Advanced Therapy Treatment Centres across South UK, driving appropriate utilisation of CAR T therapies and coordinating site qualification, setup and patient treatment logistics. Works cross-functionally with Marketing, Medical Affairs and Market Access, and is 80% field based with UK travel.

• Leeds
• On-site
• Entry level
• Permanent

Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.

Outlook · Word · Excel +1

• Newcastle upon Tyne
• On-site
• Senior

Leads and coordinates global field action management across Leica Biosystems, including recalls, corrections, removals and Field Safety Corrective Actions. Acts as global process owner and subject matter expert, partnering with Quality, Regulatory, Operations and Commercial teams on investigations, risk assessments and vigilance reporting. Also drives inspection readiness, KPI monitoring and continuous improvement across regions.

EU IVDR · ISO 13485 · FDA +1

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• Stevenage
• Hybrid
• Director · manages people

Accountable for onboarding and ongoing performance management of apheresis and treatment centres supporting clinical and commercial CAR T-cell therapies across the UK and Rest of World. Serves as the technical operations single point of contact, conducting site assessments, training centre staff, supporting quality systems and deviations, and managing process change rollouts. Involves up to 50% travel and possible management of contract employees.

Electronic Data Management Systems

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• 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