Biotechnology Jobs

Isomorphic Labs · Cambridge, United States

Lead the safety assessment strategy for small molecule and biologic drug discovery projects from inception to regulatory submission, designing screening cascades and mechanistic experiments. Partner with machine learning researchers to build predictive toxicology models and manage CRO relationships for outsourced wet-lab data generation, while mentoring junior team members.

Isomorphic Labs · London

Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.

Vertex Pharmaceuticals · London

A 12-month industrial placement within an international Medical Affairs team, supporting the planning and execution of medical projects in assigned therapeutic areas. The role involves project management, monthly dashboard reporting, managing external agencies, monitoring budgets for medical education events and advisory boards, and liaising with cross-functional and external stakeholders.

GSK · USA - Pennsylvania - Upper Providence

Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.

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.

Bicycle Therapeutics · Cambridge

Operational backbone of R&D Quality, administering and optimising a validated eQMS (Veeva, TrackWise, Dot Compliance) for GxP document control, training matrices, deviation/CAPA tracking and inspection readiness. Supports FDA, MHRA and EMA inspections and works across clinical, non-clinical and pharmacovigilance teams.

Evotec · Abingdon

Acts as the single front door between Global Biology Operations and the In Silico & AI organisation, owning demand, the in silico roadmap and delivery orchestration across computational biology, bioinformatics and AI teams. Focuses on Disease-to-Target and applying the proprietary E.MPD multi-omics resource to target identification, validation and patient stratification, while evidencing value and supporting client proposals.

Evotec · Abingdon

Acts as the single front door between Evotec's Drug Discovery Platforms and the global In Silico & AI organisation, owning demand, relationships and the in silico roadmap. Translates platform science needs across DMPK, ADME/Tox, predictive safety, screening and omics into prioritised AI requirements, then orchestrates delivery across capability units. Carries a commercial mandate, contributing to client proposals, pricing and evidencing value such as margin uplift and cycle time.