Biotechnology Jobs

• Waltham, United States
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds relationships with key external experts and represents the company at advisory boards and medical meetings.

• Stevenage
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• Swindon
• On-site
• Entry level
• Permanent

Supports the routine running of a QC Microbiology laboratory: booking in samples, maintaining reagent, media and consumable stock, ordering supplies, performing equipment checks and second-analyst checks, and helping clean classified cleanrooms. Also writes and updates SOPs, specifications and scientific reports while working to GMP standards. No previous laboratory experience is required.

Microsoft Word · Microsoft Excel

• Swindon
• Lead · manages people

Leads a team of scientific officers performing GMP QC Chemistry analysis of incoming goods, in-process, intermediate, stability and finished product samples. Acts as first escalation point for technical, compliance and personnel issues, manages batch release, stability studies, documentation and audits, and deputises for the QC Manager. Requires extensive instrumental and traditional analytical experience plus 2+ years of team leadership.

• London
• Hybrid
• £56,511 – £104,949 pa
• Mid-level

Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.

• Barcelona, Spain
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors, shaping central and site monitoring strategies across a global development portfolio. Oversee trial-data surveillance, risk reviews and signal detection using Central Monitoring technology, translating complex risk signals into actionable insights for Clinical Trial Teams. Partners with clinical, data and risk-surveillance teams to strengthen risk-based monitoring and Risk-Based Quality Management.

Artificial Intelligence

• Glasgow
• On-site
• Entry level
• Permanent

Incoming customer samples are visually inspected and recorded in a sample management system, with documentation checked to confirm correct receipt before release to testing departments. The role also involves liaising with couriers, arranging disposal of tested materials, maintaining backup samples, and managing temperature data loggers. It sits in a three-person quality team at the Glasgow science park site.

Microsoft Word · Microsoft Outlook · Microsoft Excel

• Maidenhead
• Mid-level

Unblinded monitoring of pharmacies at clinical trial sites across Scotland and the North of England, with possible additional UK and Ireland sites. Involves Investigational Product oversight, ICH-GCP compliance, eTMF documentation and acting as primary contact for pharmacy monitoring, within a sponsor-dedicated team.

eTMF

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

Manages a team of laboratory staff in a food microbiology lab, ensuring analytical procedures meet ISO17025 and UKAS standards. Responsibilities include training, appraisals, holiday and sickness management, quality assurance, equipment calibration, HSE compliance and reporting KPIs to the Laboratory Manager.

LIMS

• Oxford
• On-site
• Senior

Hands-on sole contributor owning equipment uptime and reliability in a new GMP manufacturing facility, acting as technical escalation point for technicians and contractors. Leads structured troubleshooting, RCA, CAPA ownership, CMMS data integrity, preventative maintenance planning and small capital projects, working closely with Engineering and QA. Supports 24/7 operations across early, mid and occasional night shifts with callouts, applying Lean/6S, RCM, FMEA and digital-first approaches.

CMMS · Maximo · SAP PM +5

• Leeds
• Hybrid · 3 days in office
• Entry level
• Permanent

Develops protocols and clinical study reports for early-phase trials (I-IIa), focusing on safety and pharmacokinetics. Coordinates cross-functional teams and client stakeholders to drive documents from draft to final deliverable, with on-the-job training in medical writing.

• 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.

• Macclesfield
• On-site
• Senior
• Permanent · Shift work

Provides QA leadership and GMP/aseptic expertise for aseptic manufacturing and packaging on a permanent night shift, working a 4-on, 4-off pattern. Advises on cleanroom compliance, deviations, CAPA, change control and product release, and coaches manufacturing staff on contamination control and data integrity within the Process Execution Team.

EU GMP Annex 1 · ICH Q9 · ICH Q10 +2

• 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

• Lancaster
• £33,002 – £37,694 pa

Support a collaborative project developing materials for sustainable agriculture, using materials preparation, characterisation and in vitro biological testing to study how material properties affect plant interactions. The post also involves prototype validation, health and safety implementation and laboratory work within a rapidly expanding chemistry department.