Biotechnology Jobs

• Liverpool
• On-site
• Permanent

Perform routine, non-routine and stability testing on finished pharmaceutical products at a client site, using HPLC, Dissolution, Karl Fischer and UV techniques. The role also covers technology transfers, analytical validation, GMP data review and OOS investigations, working within a managed services team embedded at the client's facility.

HPLC · Dissolution · Karl Fischer +4

• 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

• Ware
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and specification/stability recommendations across the post-approval lifecycle. Partners in a matrix with R&D, GSC, Technical and Regulatory, defends analytical product strategy in health authority inspections and embeds method knowledge into tech transfers.

PAT

• King of Prussia, United States
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and post-approval change submissions. Partners across R&D, manufacturing sites and regulatory in a matrix, embedding method knowledge into tech transfers and defending strategies during health authority inspections.

PAT

• 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

• 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.

• Stevenage
• On-site
• Mid-level

Performs complex sample preparation and quantitative analysis of small molecules and biotherapeutics using instrumentation such as GC-MS, ICP-OES, HPLC and LC-MS, supporting both GMP and non-GMP stability studies. Works largely independently to set up, maintain and troubleshoot analytical instrumentation, interpret data for technical validity and compliance, and report results to client teams. Based full-time onsite at a pharmaceutical client site as part of a functional service provider partnership.

GC-MS · ICP-OES · HPLC +2

• Hemel Hempstead
• Senior

Provides technical support and training to customers using mass spectrometry, LCMS and metabolomics platforms across EMEA. Delivers application optimisation, troubleshooting, presentations and product feedback to R&D, combining scientific expertise with customer engagement and up to 50-75% travel.

• London
• On-site
• Director
• Permanent

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

IND · CTA · BLA +1

• 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.

• 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

• High Wycombe
• Entry level
• Internship

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with SOPs and local regulatory requirements. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Microsoft Word · Microsoft PowerPoint · Microsoft Excel

• London
• On-site
• Senior
• Permanent

Processes and quality-controls paired single-cell RNA-seq and scATAC-seq data at scale, building Nextflow pipelines for custom combinatorial indexing chemistries and integrating multimodal datasets for GPU-accelerated model training. Partners with wet lab scientists and ML modellers to design evaluation frameworks and biological benchmarks, bridging experimental and computational teams in a matrixed TechBio environment.

STARsolo · Alevin-fry · Chromap +5

• New York, United States
• Remote
• Senior · manages people

Leads clinical development strategy and execution across oncology and rare disease programs, overseeing early and late-stage trials, regulatory interactions, and biomarker-driven study design. Manages teams of clinical scientists and medical directors while embedding AI, machine learning, and real-world data into trial design and evidence generation.

Recursion OS

• New York, United States
• Hybrid
• US$321,800 – US$443,080 pa
• Director · manages people

Sets enterprise strategy for clinical pharmacology, pharmacometrics and model-informed drug development across a clinical portfolio, owning dose strategy from first-in-human through registrational development. Leads quantitative approaches including population PK, PK/PD, PBPK and QSP, represents the company in health authority interactions, and builds a high-performing function within an AI-native TechBio.

Recursion OS