Biotechnology Jobs

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• London
• Hybrid
• Director

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

MHRA · Generative AI

• 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

• Swindon
• On-site
• Lead · manages people

Operates and sets up bulk formulation, filling, inspection and packing lines for sterile and non-sterile pharmaceuticals, following SOPs, BMRs and cGMP in a cleanroom environment. Performs CIP/SIP, autoclave and airlock operations, equipment monitoring and documentation, and provides team leadership on night shifts. Distinct for its aseptic manufacturing focus, hazardous materials handling and supervisory duties.

SAP · HMI · EDMS

• Waltham, United States
• Hybrid · 2 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of early clinical development medical directors and clinical scientists, owning Phase I/II clinical development plans including first-in-human, dose-escalation and proof-of-concept studies in lung and head/neck cancers. Bridges preclinical discovery and clinical development, driving translational and biomarker strategy, regulatory submissions and cross-functional matrix teams.

AI/ML

• Stevenage
• Hybrid · 2 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of medical directors and clinical scientists designing and executing early-phase oncology trials, including first-in-human, dose-escalation and proof-of-concept studies, while bridging preclinical discovery and clinical development. Accountable for clinical development plans, benefit-risk, regulatory submissions and translational biomarker strategy across lung and head/neck cancer assets.

AI/ML

• London
• On-site
• Lead · manages people

Own the manufacture of electromechanical automation systems and sterile GMP plastic consumables, driving yield, quality and cost improvements while scaling volume. Lead greenfield facility build-out, supplier and contract manufacturer management, and grow the manufacturing team alongside the Head of Engineering.

ISO 13485 · ERP · MRP +3

• Edinburgh
• Hybrid · 2–3 days in office
• £31,000 – £36,000 pa
• Mid-level
• Contract

Implement high-throughput plasmid assembly, colony PCR, Minipreps and pathway construction to build strains for hypothesis testing and model training. Work across disciplines in a lab-based, cross-pollinating team, with fortnightly research updates, mentorship and organised labbook/data keeping. Golden Gate assembly, Benchling in silico cloning and DNA sequencing are core.

Benchling · QIAgility

• Loughborough
• On-site
• Entry level
• Permanent

Performs chemical, physical and microbiological testing of raw materials, in-process, finished and stability samples in a GMP pharmaceutical QC lab. Uses wet chemistry techniques, auto titrators, Karl Fischer, FTIR and UV-Vis, plus LIMS, with instrument calibration, COSHH risk assessments and 6S housekeeping duties.

LIMS · Microsoft Office · Auto Titrators +4

• Liverpool
• Director · manages people

Leads the Operational Excellence function at a major influenza vaccine manufacturing site, deploying Lean, Six Sigma and the CSL Operating System to translate strategy into operational priorities and financial benefits. Owns the site management system, structured problem solving and continuous improvement, coaching senior leaders and leading the OE team. Reports to the Manufacturing Site Lead and sits on the Site Leadership Team.

CSL Operating System

• 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
• On-site
• Mid-level

Owns end-to-end purchasing, invoicing and inventory for both electromechanical automation systems and GMP-grade sterile fluidic consumables, spanning supplier qualification, cost-down programmes and demand planning. Reports to the Hardware Lead and works across manufacturing, biology, engineering, quality and finance, building ERP/MRP-based planning in a hands-on, on-site role.

ERP · MRP

• Abingdon
• Hybrid
• £60,000 – £75,000 pa
• Mid-level
• Permanent

National role driving new business and growing existing accounts across the UK life sciences construction market, targeting projects worth £1m-£20m in pharmaceutical, biotech, lab and healthcare facilities. Involves building relationships with end users, consultants and designers, tracking capital programmes, and working with estimating, design and pre-construction teams to shape proposals through tender and contract award.

• Macclesfield
• Permanent

Provide analytical support for drug substance manufacturing and method development, running project analysis, forced degradation studies and proof-of-concept validation. Author and review Analytical Testing Plans, method protocols and validation protocols, using HPLC and GC within a GMP-regulated lab. Work independently and in a multidisciplinary team, communicating findings to internal and external stakeholders.

HPLC · GC · NMR +4

• Cambridge
• Senior
• Temporary

Hands-on upstream process development role delivering mammalian cell culture studies, including CHO-based fed-batch and perfusion processes, media and feed optimization, and bioreactor operation from ambr systems to bench-scale stirred tanks. Works under minimal supervision within a matrix CMC team, applying DoE and statistical analysis, supporting scale-up and tech transfer to GMP and CMO partners, and providing day-to-day technical coordination to technicians and operators.

ambr · ambr250 · Stirred-Tank Bioreactors +6