Biotechnology Jobs

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

Sits within GSK's Chemical Manufacturing & Control function, running day-to-day tech transfer engagement with manufacturing sites and CMOs while redesigning processes in detail. Shapes NPI launch strategy covering site impact assessment, capacity management, digital twins, scenario planning and virtual line commissioning, and defines the target process, data and agent architecture. Owns the tech transfer package and drives agentification and MES-ready recipe building alongside forward deployed engineering pods.

MES · LIMS · ERP +6

• Stevenage
• Hybrid

Predominantly laboratory-based role planning, executing and interpreting LC-MS and LC-MS/MS experiments to characterise biopharmaceutical molecules. You will develop and troubleshoot analytical methods, investigate product quality attributes and post-translational modifications, and support early-phase programmes through forced degradation and comparability studies. Works across Discovery and CMC Development teams, with hybrid working available.

Protein Metrics · JMP · SIMCA

• Macclesfield
• On-site
• Permanent

Develops, optimises and validates trace analysis methods using LC-MS and Orbitrap technologies to detect and quantify trace-level small molecules in raw materials, intermediates and drug substances. Provides technical expertise on mutagenic impurities and nitrosamines at parts-per-billion levels, performing complex analytical investigations and authoring method development reports and validation protocols. Based at a client pharmaceutical facility, collaborating with multidisciplinary internal and external teams.

LC-MS · Orbitrap · GC-MS +6

• Guildford
• On-site
• Entry level
• Permanent

Performs analytical laboratory work on genomics samples, including sample reception, quality control, PCR preparation, and analysis, while ensuring data integrity and compliance with ISO15189 and ISO17025 standards. Maintains equipment, SOPs, training logs, and inventory, reporting issues to the Team Leader. Based in a molecular biology lab on a Monday-to-Friday shift pattern.

LIMS · QMS

• 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

• Oxford
• On-site
• Permanent

Conducts class-targeted metabolomics and metabolic engineering of plant natural products, using extraction, purification, mass spectrometry and computational structural assignment to support cell-based production of food and medicines. Works in a highly collaborative institute alongside AI and robotics teams on high-throughput analytical procedures, with stage-gated milestones and an active role in IP generation.

• Oxford
• On-site
• Mid-level

Design, build and iterate microfluidic cartridges and prototype instrumentation for a point-of-care metagenomic sequencing diagnostic. Work at the interface between cartridge design and automated actuation, running experiments on fluid behaviour, sealing and timing, and troubleshooting system-level failures alongside microfluidics, microbiology, electronics and firmware specialists.

Oracle Cloud

• Luton
• Hybrid · 3 days in office
• Senior

Lead UK direct tax compliance and reporting for a FTSE 100 biopharmaceutical group, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions. Advise the UK business on legislation changes, HMRC audits and governance regimes, while driving process efficiencies through automation and AI.

• Saffron Walden
• Hybrid
• £3,452 – £3,861 pm
• Contract

Curate molecular interaction and macromolecular complex data from scientific literature and user depositions into the IntAct and Complex Portal knowledgebases. Work with bioinformaticians and developers to build curation workflows combining expert manual curation with AI-assisted literature mining, using ontologies and community data standards.

IntAct · Complex Portal · Gene Ontology +2

• Reading
• Hybrid
• Mid-level

Supports clinical trials by designing, setting up and maintaining Interactive Response Technology (IRT) solutions, translating supply requirements into system specifications. Contributes to risk assessments, user acceptance testing and validation documentation, and advises study teams on IRT processes. Works with cross-functional global stakeholders on study startup, amendments and continuous improvement.

IRT · RTSM · IVRS +1

• Oxford
• On-site
• Mid-level
• Contract

Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.

ELISA · MSD · LIMS +2

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• Oxford
• On-site
• Senior

Sole-contributor scientist role developing and executing biochemical and molecular biology assays for PK/PD analysis, spanning genomic DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting. Works within Moderna's Clinical Bioanalytical team at Harwell, Oxfordshire, ensuring GcLP-compliant assay qualification and validation, troubleshooting with external CRO partners, and building internal and external mRNA-based bioanalytical capability.

MSD · LIMS · eLNB +1

• Oxford
• On-site
• £40,178 – £48,700 pa
• Entry level
• Contract

Conducts research characterising crosslinked proteins and lipids under a Wellcome Trust-funded grant, using proteome and lipidome methods including sample preparation, LCMS and data analysis. Manages project administration, guides junior researchers and students, and contributes to reports, publications and external seminars.

LC-MS · nanoLC-MS

• United Kingdom - Walton Oaks
• Senior

Conduct strategic regulatory activities for assigned products and markets, managing Marketing Authorisation applications, variations, renewals and NRA queries. Work with cross-functional teams and above-country hubs to maintain compliance, support clinical trial applications and share regulatory intelligence.