Biotechnology Jobs

Scientist/Senior Scientist, Mass Spectrometry - Generative Biology Institute

Develops and optimises LC-MS workflows for low-input and single-cell proteomics and/or metabolomics, supporting researchers across the institute with experiment design, method development, data acquisition and interpretation. Works closely with bioinformatics, scientific computing and AI/ML teams, and helps build SOPs and training material for single-cell MS capability.

Ellison Institute of Technology Oxford £40,000 pa

On-site Permanent

Senior Regulatory Affairs & Quality Manager

This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.

Bluetree Cambridge £65,000 – £80,000 pa

Hybrid Permanent

Trial Vendor Senior Manager - Global Clinical Operations (GCO_

Serves as the single point of contact and sub-team lead for clinical trial vendor service delivery, overseeing central labs, IRT, eCOA/ePRO, imaging and diagnostics vendors. Translates protocol requirements into vendor specifications and SOWs, manages vendor financials, KPIs and risks, and leads UAT for vendor systems within a matrixed Clinical Trial Team.

Novartis London £49,140 – £91,260 pa

Hybrid

Associate Director, Statistical Programming

Lead a global community of statistical programmers across phase I–IV clinical studies, owning programming strategy, resource allocation and validation of deliverables for complex projects or disease areas. Drives adoption of R, Tidyverse, Shiny, Git-based version control and AI-enabled tools, and acts as the statistical programming representative in submission and leadership teams.

Novartis London £67,900 – £126,100 pa

Hybrid Permanent

GLP Vendor Oversight and QA Lead

This role involves overseeing the quality and compliance of external partners in GLP-regulated nonclinical research, including CROs and laboratories. Responsibilities include vendor qualification, risk-based monitoring, audit coordination, and ensuring adherence to regulatory standards. The role requires deep knowledge of GLP, GCP, and GMP regulations and strong cross-functional collaboration.

CSL Holly Springs, United States