Biotechnology Jobs

Isomorphic Labs · Cambridge, United States

Lead in vitro and cellular pharmacology strategy for small-molecule drug design programs, defining screening cascades and guiding biophysical, biochemical and cell-based assays from hit identification to candidate selection. Bridge computational AI/ML predictions with laboratory validation, managing CRO partnerships and collaborating with chemistry, structural biology and translational teams.

Isomorphic Labs · Cambridge, United States

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

Basecamp Research · London

Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.

Moderna · Oxford

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

IQVIA · Reading

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.

GSK · London · US$340,500 – US$567,500 pa

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability and chairing a cross-functional matrix Medicine Development Team spanning clinical, translational, regulatory, manufacturing and commercial. Drives strategy, go/no-go decisions and lifecycle plans for novel vaccine platforms such as mRNA and neoantigen-based therapies.

Moderna · Oxford

Provides hands-on MS&T engineering expertise across drug substance manufacturing and label, packaging and final-storage operations at the Harwell site. Leads technology transfer, process start-up, validation, continued process verification and troubleshooting, authoring protocols and reports as an individual contributor. Works cross-functionally with Manufacturing, Quality and Supply Chain, with on-call or shift coverage as required.

IQVIA · Cambridge

Hands-on bioanalytical role developing, optimising and running LC-MS/MS assays for small and large molecule DMPK studies in an early discovery setting, analysing matrices such as plasma, blood, brain, bile, faeces and urine. Combines complex mass spectrometry troubleshooting and method development with leading scientific projects, mentoring colleagues and driving novel assay innovation in a matrix team.

HAYS Specialist Recruitment · Cambridge · £80,000 – £120,000 pa

Lead complex clinical technology transformation and data migration programmes across the clinical trial ecosystem, covering CTMS, eTMF and study startup systems. Drive data mapping, validation, reconciliation and cutover while partnering with Clinical Operations, Quality, Regulatory, CROs and vendors globally. Highly visible role supporting acquisitions, integrations and system consolidations with a focus on compliance and data integrity.

Ipsen · London

Leads one or more Early Development Asset Teams, owning integrated strategy from candidate nomination through first-in-human trials across preclinical, translational, clinical, regulatory and CMC workstreams. Serves as scientific champion for oncology assets, presenting data and investment recommendations to governance bodies and contributing to in-licensing due diligence.

Danaher · Portsmouth

Responsible for new product development and improvement projects for hardware and disposable devices used in the biotech industry, taking initiatives from spec definition through design, testing and validation to manufacturing transfer. Provides technical leadership on complex engineering challenges, applies 3D CAD design, manages project plans and resources, and reports progress to leadership. On-site role with up to 20% international travel.

Newton Colmore · Cambridge

Design, build and test the hardware of a novel biotech manufacturing device, working with 3D CAD (ideally SOLIDWORKS) alongside physicists, scientists, electronics and design engineers. The role spans proof of concept through development and testing of complex electro-mechanical, mechatronic or precision technology, with exposure to third-party meetings and industry conferences.

Newton Colmore · Cambridge

Design, build and test the hardware of a novel biotech manufacturing device, taking it from proof of concept through development and testing. Works in a multidisciplinary team of physicists, scientists, electronics and design engineers, using 3D CAD (ideally SOLIDWORKS) on mechatronics, automation, robotics or precision electro-mechanical technology. Involves third-party meetings and attending biotech and medical device conferences, suiting someone comfortable wearing multiple hats in a start-up.

Nuclera · Cambridge

Formulate, dispense and quality-control reagents for a protein discovery platform, operating lab equipment such as pipettes, centrifuges and UPLC systems. The role covers batch documentation, inventory management via ERP and troubleshooting production deviations, working closely with R&D, QA and Supply Chain in a fast-paced lab environment.

Nuclera · Cambridge

Full-stack engineer building customer-facing cloud and instrument software plus internal tools supporting in-house protein screening services. Owns features end to end, from gathering requirements with biologists and stakeholders through technical design, implementation and testing across backend, frontend, dev-ops and QA.