Biotechnology Jobs

• London
• Hybrid
• Director · manages people

Leads GSK's Forward Deployed Engineering function for CMC R&D, setting strategy, hiring and mentoring engineers, and owning senior BU sponsor relationships. Personally contributes to strategic engagements building digital twins, physical AI and self-driving lab capability, using AI coding agents as the primary development mode.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• 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.

• New York, United States
• Hybrid · 2–3 days in office
• US$151,800 – US$220,660 pa
• Senior

Integrate phenomics, transcriptomics, genomics and proteomics data to nominate novel targets and validate immunology and inflammation disease biology, piloting new methods for target discovery and early patient population hypotheses. Partner cross-functionally with biologists, chemists, data scientists and engineers to build data packages that drive program milestones and investment decisions.

Python · R · CRISPR

• New York, United States
• Hybrid · 2–3 days in office
• US$151,800 – US$220,660 pa
• Senior

Integrates phenomics, transcriptomics, genomics and proteomics data to nominate and validate oncology targets and define precision oncology patient strategies. Partners cross-functionally with biologists, chemists, engineers and translational experts to build target data packages and pilot novel discovery methods, including agentic target packages and mechanism-of-action work.

CRISPR

• 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

• Cambridge
• Lead

Lead developability science across drug discovery programmes, designing and interpreting preformulation, solid-state and biopharmaceutic studies and integrating experimental, computational and AI-enabled approaches to guide candidate progression. Act as primary scientific client contact, lead projects from proposal to delivery, support business development and mentor junior scientists within a growing Cambridge team.

PBPK · DCS · Spray Drying +2

• Slough
• Hybrid · 3 days in office
• £37 – £50 ph
• Contract

Process, analyse and interpret omics data from clinical portfolio studies to uncover biological mechanisms, treatment effects and safety signals. Develop analysis pipelines using state-of-the-art tools, document reproducible code for patient-level data, and write reports and scientific publications. Requires strong bulk and single-cell RNAseq expertise, R, HPC/Unix and Docker skills.

Docker · DNAnexus

• Hyderabad, India
• On-site
• Director · manages people

Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.

• Home Worker - NORTHERN IRELAND
• Remote
• Director · manages people

Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across development, validation and deployment.

• 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

• 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

• 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.

• London
• Hybrid
• Junior
• Permanent

Hands-on business development role researching pharma and biotech accounts, writing outreach, and owning CRM pipeline hygiene in HubSpot. Works directly with founders and the head of sales, building sales materials and AI workflows while coordinating with the science team ahead of customer meetings.

HubSpot · LinkedIn

• 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
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4