Biotechnology Jobs

• Oxford
• On-site
• Senior
• Permanent

Perform plant transformation and regeneration workflows, optimising tissue culture protocols across crops and genotypes while troubleshooting regeneration failures and contamination. Track transformation efficiency, mentor junior technicians, and maintain rigorous documentation standards. Work closely with Transformation Scientists in a fast-moving, interdisciplinary plant science institute.

• Oxford
• On-site
• Senior
• Permanent

Lead the development and optimisation of molecular biology workflows—nucleic acid extraction, purification, library preparation and sample processing—for integration into a fluidic, cartridge-based diagnostic device. Work at the intersection of biology, chemistry and engineering, using Design of Experiments and quantitative methods to reduce technical risk and guide the platform from proof-of-concept to prototype.

Whole Genome Sequencing · Oracle Cloud

• Stevenage
• Director

Leads Quantitative Systems Pharmacology and QST modelling within GSK's Clinical Pharmacology and Quantitative Medicine group, building mechanistic mathematical models of disease, drug action and trial design. Defines clinical pharmacology strategy across the Respiratory, Immunology and Inflammation portfolio, working with biologists, clinicians, statisticians and AI/ML colleagues. The role sits in a newly formed Centre of Excellence for Model-Informed Drug Development, initially in Stevenage with a planned move to Cambridge.

• Grimsby
• US$188,100 – US$313,500 pa
• Director

Leads quantitative systems pharmacology and QST modelling within a clinical pharmacology and quantitative medicine group, building mechanistic models of disease and drug action and running simulations to inform trial design. Defines and coordinates MIDD strategies across respiratory, immunology and inflammation programmes, working with biologists, clinicians, pharmacometricians and statisticians. Combines inverse-problem modelling, scientific ML and statistical methods to support decisions from exploratory research through clinical development.

• Opfikon, Switzerland
• Lead · manages people

Provides medical and scientific expertise on clinical safety across a product's lifecycle, with emphasis on signal detection, risk management and regulatory submissions. Chairs the Safety Management Team, oversees aggregate reports such as DSURs, PSURs and RMPs, and acts as the safety representative in cross-functional development and post-marketing teams.

DSUR · PSUR · RMP +3

• London
• On-site
• Director

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.

Generative AI

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2