Biotechnology Jobs

• Liverpool
• On-site
• Permanent

Perform method development and proof-of-concept validation on pharmaceutical raw materials, intermediates and drug substances, mainly APIs, using HPLC, GC and MS. Support technology transfers for novel substances, review data for compliance, investigate OOS/OOE results and document work to client procedures. Based on-site at a client facility as a managed PSS scientist, liaising with client representatives and supporting audits and continuous improvement.

HPLC · GC · MS +7

• Grimsby
• On-site
• Entry level
• Permanent

Analyse food samples using microbiological techniques, including media preparation, plate reading, and result validation, while maintaining UKAS and ISO quality standards. Work a 2-on-2-off shift pattern covering 37.5 hours per week, with responsibility for HSE compliance and liaising with Customer Services on technical matters.

• USA - Pennsylvania - Upper Providence
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, including budget, forecasting, cost controls and retiring under-used sources. Manages vendor relationships and commercial terms, maintains copyright-compliant governance and user guidance, and works across scientific, procurement, legal, digital and technology teams to make licensed content AI- and text-mining-ready.

Excel · PowerPoint · Word +2

• Barnard Castle
• Senior · manages people

Acts as the business-technology integrator between GSK functions and CDMO partners, leading the global External Manufacturing digital and technology roadmap. Owns end-to-end delivery of integration, Smart Manufacturing and AI-enabled solutions, from business case and prototyping through adoption, service transition and value realisation, while embedding Responsible AI, GxP and cybersecurity requirements.

Factory Integration Layer · Product Development & Lifecycle Management · GxP +1

• London
• On-site
• £33,000 – £38,000 pa
• Mid-level
• Permanent

This role involves hands-on troubleshooting, maintenance, calibration, and repair of medical equipment both onsite and remotely within a leading hospital environment. The engineer will perform preventative maintenance, equipment upgrades, and ensure compliance with manufacturer guidelines and contractual KPIs. Strong diagnostic skills and the ability to explain technical issues clearly to non-technical stakeholders are essential.

• 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

• Bracknell
• Hybrid · 2–3 days in office
• £37 – £49 ph
• Senior
• Contract

Analyse large-scale single-cell, bulk transcriptomics and other omics datasets, and develop new computational methods to extract biological insight. Build scalable, well-tested software and workflows for atlas-scale data (millions of cells) and high-dimensional proteomics, acting as the analytical point of contact in multidisciplinary collaborations from analysis plan through to publication or portfolio decision.

Visium · Xenium · MERFISH +4

• London
• On-site
• Mid-level

Develops and optimises therapeutic delivery formulations, designing lab experiments to assess stability, physicochemical properties and in vitro performance. Works in a multidisciplinary biotech team, characterising formulations analytically and supporting scale-up and tech transfer towards manufacturing. Distinct for its blend of formulation science, experimental development and translational research.

• United Kingdom
• Remote
• Lead

Leads the design and implementation of bioanalytical strategies for a client-dedicated global biopharma team, ensuring lab-based activities align with context of use. Manages experimental design, tech transfer and regulatory submissions, interacting with lab scientists, cross-functional groups and Health Authorities in a matrix environment.

ddPCR · qPCR · RT-qPCR +6

• Sheffield
• Remote
• Senior

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

SAS · R

• 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

• Opfikon, Switzerland
• Senior

Leads safety review and end-to-end signal detection across a product's lifecycle, using quantitative and qualitative methods alongside Global Safety Leads. Contributes to aggregate safety reports, risk management plans and regulatory responses, and mentors junior PVS staff. Works cross-functionally with Development, Medical Affairs and Regulatory teams on vaccine and national-significance products.

Microsoft Excel

• Maidenhead
• Senior

Leads safety surveillance and signal detection across a product's lifecycle, reviewing clinical and post-marketing data and contributing to aggregate safety reports and risk management plans. Partners with Global Safety Leads and cross-functional teams, mentors junior scientists, and supports regulatory responses.

Microsoft Excel

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

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.

Artificial Intelligence

• Dublin, Ireland
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence