Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Accountable for end-to-end clinical development strategy for an antibody-drug conjugate asset across multiple tumour types, from first-in-human through registrational trials and launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial.

• London
• Hybrid · 2 days in office
• US$202,500 – US$371,250 pa
• Director · manages people

Leads clinical development strategy for hepatology assets within GSK's Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and regulatory interactions across all development phases. Hybrid role with at least two on-site days weekly.

• London
• Hybrid · 3 days in office
• Lead · manages people

Lead a team of biologists in the Exploratory Sciences group, owning in vitro pharmacology strategy for novel modalities such as TPD, molecular glues and peptides. Design screening cascades and quantitative assays, manage CRO studies, and champion LLM agentic workflows and in silico hypothesis building alongside ML and engineering colleagues.

SPR · GCI · nanoDSF +5

• London
• Hybrid · 3 days in office
• Senior · manages people

You will design and develop LLM applications for drug discovery, working with research scientists and engineers on model architectures, post-training, reasoning, agents and reinforcement learning. The role spans core ML research, scaling training and inference frameworks, and potentially leading standalone projects with technical mentorship.

JAX · PyTorch · TensorFlow +3

• Oxford
• On-site
• Entry level
• Permanent

Postdoctoral role in the joint Monera project, building multi-modal generative models of whole organisms starting with E. coli. You will perform high-throughput genome engineering to generate diverse microbial strains and design scalable measurement strategies, working in an integrated computational and experimental team alongside AI scientists.

Escherichia coli

• Oxford
• On-site
• Entry level
• Permanent

Design and conduct experiments on nanopore technologies, single-molecule analysis, and 3D tissue engineering, spanning chemistry, biology, physics and engineering. Postdocs lead development of emerging biotech methods, publish impactful research, and mentor junior researchers within a 100+ researcher institute.

3D Printing

• London
• Lead

Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.

• Cambridge
• Senior

Acts as subject matter expert for stem cell culture technologies, leading development, optimisation and delivery of cellular systems for drug discovery. Manages multiple cell culture programmes, supplies high-quality cell batches for high-throughput screening, and troubleshoots assays while ensuring biological safety compliance. Collaborates with multidisciplinary teams and external partners across global sites.

Automated Liquid Handling Platforms · High-Throughput Screening

• Maidenhead
• Mid-level

Monitors and oversees clinical trial sites across the Midlands, handling site initiation, monitoring visits and closeouts while ensuring GCP compliance and patient safety. Also supports feasibility assessments, investigator recruitment, vendor coordination, SAE reporting and mentoring of junior team members within a global FSP team.

• Didcot
• On-site
• Lead · manages people

Lead a team of software engineers delivering next-generation Raman spectroscopy software from the Laser Spectroscopy Center of Excellence in Oxford (Harwell). The role owns R&D operations across the software product lifecycle, solving engineering challenges and integrating hardware and software with global partners, using modern architectures such as containerisation, Kubernetes, microservices and cloud deployment.

Kubernetes · Linux · Microsoft

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.

• Stevenage
• On-site
• Mid-level

Performs complex sample preparation and quantitative analysis of small molecules and biotherapeutics using instrumentation such as GC-MS, ICP-OES, HPLC and LC-MS, supporting both GMP and non-GMP stability studies. Works largely independently to set up, maintain and troubleshoot analytical instrumentation, interpret data for technical validity and compliance, and report results to client teams. Based full-time onsite at a pharmaceutical client site as part of a functional service provider partnership.

GC-MS · ICP-OES · HPLC +2

• Seqirus USA - NC - Holly Springs
• Lead

Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the full vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and governance forums. Coordinates inspection readiness and audit support, ensures compliance with GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and ALCOA+ data integrity, and leads vendor risk assessments such as FMEA and risk registers.

OECD GLP · 21 CFR Part 58 · Annex 11 +3

• Maidenhead
• Lead

Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and inspection readiness. Ensures adherence to GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and data integrity (ALCOA+), partnering with Nonclinical Development, Procurement, Legal and IT.

OECD GLP · 21 CFR Part 58 · Annex 11 +3

• Guildford
• £48,337 – £70,878 pa
• Senior
• Permanent

Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UKRI/NIHR/Wellcome funding, publish high-impact work, and teach AI and data science at undergraduate and postgraduate level.