Biotechnology Jobs

• Stevenage
• Hybrid
• US$232,650 – US$387,750 pa
• Director · manages people

Leads CMC's scientific data, application and agentic AI product portfolio, setting integrated strategy and roadmap across forward-deployed engineering, product management and AI product strategy. Accountable for delivery, GxP compliance, data governance, budget and headcount, and for representing the capability to R&D, supply chain and quality leadership.

Python

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$232,650 – US$387,750 pa
• Director · manages people

Leads CMC's scientific data, application and agentic AI product portfolio, owning strategy, roadmap, governance and GxP compliance across forward-deployed engineering, product management and AI teams. Manages budget, headcount and external partners while representing the capability to R&D, supply chain and quality leadership.

Python

• 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

• 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

• Cambridge
• Director

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.

Veeva Vault · Planisware · Signavio +2

• Maidenhead
• Mid-level · manages people

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

• London
• Hybrid
• Director · manages people

Leads the global and US Medical Affairs Neuro-Oncology team, owning medical strategy, evidence generation and launch planning for pipeline and marketed assets. Serves as a key interface between Medical Affairs and R&D, clinical development and commercial functions, representing regional insights in governance forums. Combines people management with hands-on execution across a complex matrix.

• London
• Hybrid
• Director
• Permanent

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.

NONMEM · R · Monolix +3

• Cambridge
• Hybrid · 3 days in office
• Director · manages people

Owns International regulatory strategy for complex cell therapy programs, embedding regional requirements into evidence generation, submissions and labeling. Leads BLA/MAA planning, Health Authority engagements and labeling negotiations, integrating clinical, CMC, safety and commercial input. Also leads a matrix regulatory team, coaching colleagues and shaping policy and process improvements.

BLA · MAA · IND +2

• Stevenage
• Hybrid
• £26,000 – £40,000 pa
• Mid-level
• Permanent

Field-based role installing, maintaining and servicing nano-flow cytometry instruments at customer sites across the UK and Europe, plus remote phone and email troubleshooting of hardware, software and reagents. Involves preventative maintenance scheduling, service documentation, spare parts inventory and coordinating service contracts with the sales team, following training with senior technical staff.

Nano-flow Cytometry · nFCM

• Grimsby
• On-site
• Lead · manages people
• Permanent

Manages a team of laboratory staff in a food microbiology lab, ensuring analytical procedures meet ISO17025 and UKAS standards. Responsibilities include training, appraisals, holiday and sickness management, quality assurance, equipment calibration, HSE compliance and reporting KPIs to the Laboratory Manager.

LIMS

• Grimsby
• On-site
• Entry level
• Permanent

Analyse food samples using microbiological techniques, including media preparation, plate reading, and result validation, while maintaining UKAS and ISO quality standards. Work a 2-on-2-off shift pattern covering 37.5 hours per week, with responsibility for HSE compliance and liaising with Customer Services on technical matters.

• Sheffield
• £32,722 – £37,369 pa
• Senior
• Contract

You will process samples for molecular and genomic analysis, maintain laboratory equipment, and support visiting researchers in a Genomics Laboratory. The role also involves training users new to molecular biology, advising external clients, and contributing to research and development that expands the facility's capabilities.

eDNA

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• London
• On-site
• £33,000 – £38,000 pa
• Mid-level
• Permanent

This role involves hands-on troubleshooting, maintenance, calibration, and repair of medical equipment both onsite and remotely within a leading hospital environment. The engineer will perform preventative maintenance, equipment upgrades, and ensure compliance with manufacturer guidelines and contractual KPIs. Strong diagnostic skills and the ability to explain technical issues clearly to non-technical stakeholders are essential.