Biotechnology Jobs

• Addlestone
• £47,557 pa
• Permanent

Assesses quality data submitted by companies to support marketing authorisation applications and variations for veterinary medicines, as part of the Quality team within the Pharmaceuticals Section. Also contributes to regulatory science strategy, guideline development, product defect assessment and international training of other regulators.

Microsoft Office 365 · Word · Excel +3

• Stevenage
• On-site
• Entry level

Support GMP compliance in a multi-product cell and gene therapy facility, reviewing batch manufacturing and QC records, managing controlled documentation, and preparing patient-specific labels. Work with cross-functional teams on batch release, quality events and inspection readiness, on a Sunday–Wednesday shift pattern.

• Belfast
• £35,000 – £37,532 pa
• Entry level
• Contract

A graduate-level KTP Associate role based at Norbrook Laboratories, working within the R&D team to develop a data-driven framework for pharmaceutical scale-up of liquid dosage veterinary medicines. The project focuses on predictive modelling of process parameters and product quality across scales, combining chemical engineering principles with statistical and hybrid data modelling, delivered in collaboration with Queen's University Belfast's School of Pharmacy.

• Ware
• On-site
• Mid-level

Ensures manufacturing and warehouse operations comply with SOPs, cGMP and UK/EU regulatory requirements, investigating deviations and managing CAPA, complaints and change control. Provides quality oversight of facilities, equipment and personnel, coaching staff and running GEMBA and process confirmation activities at a respiratory inhaler and oral solid dose site.

• Abingdon
• On-site
• Entry level
• Permanent · Shift work

Operate pilot plant reactors and ancillary equipment in a GMP-regulated large-scale chemical production environment, running multiple syntheses, some never previously scaled. Duties include routine maintenance and reconfiguration of reaction vessels, environmental monitoring, accurate batch documentation, and shift handovers. The role follows a rotating 12-hour day and night shift pattern averaging 42 hours per week.

Microsoft Office

• London
• Hybrid
• Senior

Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.

LIMS

• 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

• London
• Lead

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Quality Risk Management System

• London
• Hybrid
• £63,917 – £118,703 pa
• Director

Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.

DHT · SaMD · SaaS +1

• Oxford
• On-site
• Mid-level

Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.

LabVantage · LIMS · Generative AI

• London
• Hybrid · 2–3 days in office
• Mid-level

Delivers performance analysis, market intelligence and targeted market research to help the Europe & International leadership team make commercial decisions. Combines internal performance data, customer engagement analytics and external insights to explain results, identify risks and growth opportunities, and lead priority qualitative and quantitative studies. Works in a matrix with Global Data & Analytics and research teams, with two to three days a week onsite in London.

Global CX Tools

• 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.

• Swindon
• Entry level
• Internship

Support the QC Chemistry team by performing routine analytical testing of incoming goods, intermediates and finished products under cGMP conditions. Duties include stock control of reagents and reference standards, equipment checks, calibration and preventative maintenance, reagent preparation, glassware washing, waste disposal and maintaining technical documentation and training records.

pH Meters · Balances

• Reading
• Senior

Embedded with a global pharmaceutical sponsor, you own end-to-end clinical supply strategy across complex trials: protocol interpretation, label text, demand forecasting, packaging, IRT setup, distribution and temperature-excursion management. You lead vendor oversight, risk assessments and budget tracking while advising study teams and client leadership.

IRT · RTSM · ERP +3

• Cambridge
• Director · manages people

Lead a biometrics team delivering statistical design, analysis and interpretation for oncology product development, from preclinical studies through regulatory submissions and health technology assessment. Represents statistical strategy at internal governance and external bodies such as health authorities and advisory boards, while mentoring statisticians and partnering with CROs.

SAS · R · Python