Biotechnology Jobs

Basecamp Research · London

Owns the peptide and protein platform as a commercial product, spanning market and competitive intelligence, target product profiles, roadmap and packaging decisions, and go-to-market positioning. Sits between model, data and science teams and business development, and is accountable for partner engagement and revenue generation. Requires deep peptide therapeutics and licensing deal expertise.

Basecamp Research · London

Runs a high-throughput sample processing pipeline, performing DNA extraction, normalisation and library preparation on soil, faecal and other environmental samples. Operates automated liquid handling platforms such as Myra9, logs everything in Benchling LIMS, and carries out QC checks while supporting R&D protocol testing in a CL2 lab.

Mytos · London

Owns all aspects of hardware design for automated cell-production machines, from concept through to manufacture, improving robustness and reliability. Leads development of systems interfacing with optics and fluidics, refines test rigs and quality processes, and helps shape engineering culture. Based on-site in the lab at Imperial College's White City innovation hub.

Mytos · London

Open general application for a London-based biotech automation company building machines that fully automate human cell production. The team, drawn from ex-Dyson engineers and Nature-published scientists, seeks people with a track record of solving hard technical or non-technical challenges, low ego and high curiosity, including those starting their first job.

Moderna · Oxford

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

Newton Colmore · Cambridge

Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, experimental design, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.

Moderna · London

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.

SRG · Loughborough · £14 – £15 ph

Perform analytical testing for batch release, stability studies and complaint investigations in a GMP/GLP-regulated pharmaceutical lab, using techniques such as HPLC and UV spectroscopy. Support OOS/OOT investigations, maintain Good Documentation Practices, review and issue GMP documentation, and help with calibration and equipment maintenance. A 12-month temp contract within a cross-functional QC team.

Evotec · Abingdon

Owns Evotec's in silico therapeutics design capability, uniting computational chemistry, generative and modality design (small molecules, peptides, protein engineering, degraders, molecular glues) and predictive ADMET/safety under one mandate. A newly created unit within the In Silico & AI group with an explicit build mandate: set technical vision, grow a multi-site team, and industrialise repeatable, benchmarked methods across partner programmes.

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 · London

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.