Biotechnology Jobs

• Oxford
• On-site
• Lead · manages people
• Permanent

Build and oversee plant growth and phenotyping facilities, ensuring controlled, reproducible environments in growth chambers and greenhouses. Hands-on player-coach role covering planting, irrigation, pollination, sampling and harvest, plus pest and pathogen management, GMO compliance and phenotype data capture. Also shapes field trial operations and future team hiring.

Controlled Environment Growth Chambers · Greenhouses

• Oxford
• On-site
• Entry level
• Permanent

Hands-on laboratory role supporting microbiology, molecular biology, sample processing and sequencing within the Pathogen Applications Team. Involves receiving and tracking clinical samples, preparing microbial cultures, running qPCR and sequencing workflows, and maintaining QC and documentation. Suits an early-career scientist with practical lab experience in a diagnostic or high-throughput environment.

Sequencing · Oracle Cloud

• Waltham, United States
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO

• Rockville, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Swindon
• On-site
• Shift work

Operate aseptic filling lines and manufacture pharmaceuticals to SOPs and Batch Manufacturing Records, performing filling, packaging, in-process checks, line changeovers and cleaning. Work in cleanrooms on Double Days, 24/7 or Night shifts, using HMI-controlled CIP/SIP systems, autoclaves and SAP, and support validation and new product introduction.

SAP · HMI · CIP +2

• 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

• Warrington
• On-site
• Senior
• Permanent

Contributes to manufacturing sciences by ensuring manufacturing quality, process validation and regulatory compliance for biopharmaceutical and diagnostic products. Develops and implements CMC strategies, standardises procedures and drives process improvements, while mentoring technical staff and leading cross-functional teams in a regulated GMP environment.

FDA · EMA

• Uxbridge
• Hybrid
• Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

• Oxford
• On-site
• Entry level
• Temporary

Operate manufacturing equipment for mRNA vaccine production under cGMP and SOPs, maintaining documentation, gowning and housekeeping standards. Partner with Quality Assurance on batch disposition, lead root cause analysis and CAPA for deviations, and troubleshoot equipment and digital system issues. Work 100% onsite with digital and Generative AI-enabled manufacturing technologies.

Generative AI

• Portsmouth
• On-site
• Entry level
• Permanent

Performs laboratory test work in line with SOPs, recording raw data and flagging delays or deviations to management. Reviews testing requirements and safety data, troubleshoots instrumentation, and helps maintain lab systems such as purchasing, calibration and materials inventory. Based on-site in Portsmouth within a validation and lab operations team.

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.

• Uxbridge
• Director · manages people

Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.

• Slough
• On-site
• Mid-level
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances in a client's Analytical Service Department, running ELISA, cell-based and Biacore assays and capturing data in laboratory software and electronic notebooks. Generates and reviews GMP-compliant documentation, SOPs and protocols, supports method development and validation, and handles out-of-specification investigations while liaising with internal and external clients.

Biacore · Vi-Cell · Microsoft Office

• Slough
• On-site
• Senior
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances using ELISA, cell-based potency assays and Biacore (SPR), while coordinating assay activities and managing project priorities and timelines. Acts as a technical subject matter expert, mentoring colleagues and supporting method development, validation, troubleshooting and GMP-compliant documentation within a client-facing analytical service department.

ELISA · Biacore · Vi-CELL +2

• Cambridge
• Director

Leads business process mapping, design and optimisation across CMC Regulatory Affairs, from development and registration through post-approval lifecycle management. Partners with IT, data owners and cross-functional teams to translate regulatory needs into digital, automation and AI use cases, then drives implementation, adoption and KPI measurement. Distinct for combining regulatory operations expertise with AI-enabled capability building in a global matrixed pharma environment.

Veeva Vault · Planisware · Signavio +2