Biotechnology Jobs

GSK · Belgium-Wavre · €141,000 – €235,000 pa

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix.

GSK · Siena, Italy · €124,500 – €207,500 pa

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.

Moderna · Oxford

Provides hands-on MS&T engineering expertise across drug substance manufacturing and label, packaging and final-storage operations at the Harwell site. Leads technology transfer, process start-up, validation, continued process verification and troubleshooting, authoring protocols and reports as an individual contributor. Works cross-functionally with Manufacturing, Quality and Supply Chain, with on-call or shift coverage as required.

Moderna · London

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

Bristol Myers Squibb · Uxbridge

Lead statistical programming for clinical trials, turning complex data into submission-ready outputs using SAS, CDISC, and ADaM standards. Embedded in cross-functional teams, you'll review analysis plans, shape programming strategy, and mentor other programmers while supporting major regulatory filings.

Gilead Sciences · Cambridge

Leads business process mapping, design and optimisation across CMC Regulatory Affairs, from development and registration through post-approval lifecycle management. Partners with IT, data owners and cross-functional teams to translate regulatory needs into digital, automation and AI use cases, then drives implementation, adoption and KPI measurement. Distinct for combining regulatory operations expertise with AI-enabled capability building in a global matrixed pharma environment.

Ipsen · London

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Ipsen · London

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Relation Therapeutics · London

Lead clinical pharmacology and pharmacometrics across a growing drug discovery portfolio, serving as the quantitative lead on cross-functional project teams. Apply MIDD, PBPK, population PK/PD and QSP modelling to translate nonclinical data into human dosing and trial design, spanning small molecules, biologics and novel platforms. Also manages CRO partnerships and authors regulatory submissions.

Gilead Sciences · Uxbridge

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Thermo Fisher Scientific · Swindon

Leads a team of scientific officers performing GMP QC Chemistry analysis of incoming goods, in-process, intermediate, stability and finished product samples. Acts as first escalation point for technical, compliance and personnel issues, manages batch release, stability studies, documentation and audits, and deputises for the QC Manager. Requires extensive instrumental and traditional analytical experience plus 2+ years of team leadership.