Latest Pharmaceutical Scientist Jobs

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within oncology clinical development, specifically in genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, contribute to study design and regulatory interactions, and interpret clinical data to inform decision-making. They will work closely with cross-functional teams and external experts to advance GSK’s oncology pipeline with a focus on high unmet need areas.

GSK Switzerland

Hybrid Permanent

Medical Director, Oncology Clinical Development - GU

This role involves leading medical oversight and clinical strategy for genitourinary (GU) oncology trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and scientific integrity. They collaborate with cross-functional teams and external experts to advance innovative cancer treatments through clinical development.

GSK £189,750 – £316,250 pa

Field Service Engineer, Medical Diagnostic Systems

A Field Service Engineer will maintain and repair advanced medical diagnostic systems in NHS and private laboratory settings, providing on-site technical support and troubleshooting. The role involves regular weekend work and extensive customer interaction with laboratory staff. Full product training is provided, emphasizing customer service and technical excellence in a high-reliability healthcare environment.

TRS Consulting Trowbridge, Wiltshire, BA14 8EY, United Kingdom £52,000 pa

On-site Permanent

Manager, Global Regulatory Science CTA

Lead the operational execution of Clinical Trial Applications (CTAs) globally outside the US, with a focus on compliance, submission excellence, and cross-functional coordination. Serve as the subject matter expert for the UK clinical trial regulatory landscape, including MHRA requirements and evolving legislation. Leverage digital platforms and AI-enabled tools to enhance regulatory operations and submission efficiency across international markets.

Moderna

On-site Permanent

Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent

Senior Director, Targets and Mechanisms Solutions

Leads strategic direction and AI-driven innovation for Pfizer’s Targets and Mechanisms platforms, overseeing global teams to deliver scalable digital solutions that accelerate drug discovery. Focuses on integrating advanced data technologies, omics analytics, and predictive systems to support therapeutic target identification across research units. Works closely with R&D and digital stakeholders to align technology roadmaps with scientific and clinical priorities.

Pfizer £230,900 – £384,800 pa

Senior Director, Targets and Mechanisms Solutions

Lead the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, delivering scalable, science-centric digital solutions to accelerate drug discovery. Oversee a global team integrating advanced data technologies, AI, and predictive analytics across research units including Oncology, Vaccines, and Inflammation & Immunology. Shape translational biomarker frameworks and target identification strategies using large-scale omics, clinical data, and competitive intelligence to de-risk development and inform clinical decisions.

Pfizer £230,900 – £384,800 pa

Director, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategies for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality submissions including INDs, NDAs, and IMPDs across US, EU, and ROW regions. Provide strategic guidance on regulatory requirements, support clinical trial materials, and ensure compliance with evolving GMP standards.

Recursion London, W1C 2QP, United Kingdom £111,100 – £141,800 pa

Remote Permanent

Senior Executive Assistant to CEO

Provide high-level executive support to the CEO of a clinical-stage TechBio company, managing a complex calendar, international travel, and communications while serving as a key liaison across global teams and stakeholders. Enable strategic priorities through proactive coordination of board meetings, investor events, and cross-functional initiatives in a fast-paced biotechnology environment. Operate with discretion and precision in a mission-driven organization focused on accelerating drug discovery through AI and industrialized biology.

Recursion North Tyneside, NE29 8EP, United Kingdom US$130,460 – US$164,780 pa

On-site Permanent

Process Operators, Pharmaceutical, nights

Operate and assemble single-use pharmaceutical products in a regulated cleanroom environment, following strict SOPs and quality procedures. Perform in-process inspections, documentation, and product testing while adhering to cGMP standards. Support continuous improvement and collaborate with quality and engineering teams to resolve issues.

NMS Recruit Ltd t/a Russell Taylor Group Speke, Merseyside, United Kingdom £29,000 – £31,000 pa

Production Chemist

Production Operative (Pharmaceutical Manufacturing)KentPermanent and Full-time roleIntroductionOur client is a growing pharmaceutical manufacturer supplying Active Pharmaceutical Ingredients (APIs) and specialist products to the pharmaceutical and nutraceutical sectors. Due to continued expansion, they are seeking aProduction Operative to join their manufacturing...

Reed Ct139Nd, CT13 9ND, United Kingdom

Production Chemist

This role involves operating manufacturing equipment and handling raw materials in a GMP-regulated pharmaceutical environment. The candidate will prepare and document batch production processes while ensuring compliance with strict quality, safety, and regulatory standards. It is a hands-on position within a close-knit team focused on producing high-quality APIs and specialist products.

Reed Ct139Nd, United Kingdom

Legal Counsel - Pharma/Life Sciences (12-month

Your new companyA global pharmaceutical and life sciences organisation is seeking an experienced Legal Counsel to join its UK & Ireland legal team on a 12-month contract. Operating at the forefront of healthcare innovation, the business develops and delivers medicines,...

Hays Legal Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £450 – £580 pd

Contract

Quality Assurance Officer

This role involves reviewing batch manufacturing and packaging records to ensure compliance with GMP standards prior to product release, supporting batch release activities, and maintaining quality documentation. The candidate will collaborate with external contract manufacturers and internal teams within a virtual pharmaceutical model. The position offers exposure to pharmaceutical products and medical devices across European markets, with a hybrid working arrangement.

Walker Cole International London, United Kingdom £30,000 – £35,000 pa

Production Manager - Pharmaceuticals

Lead and manage pharmaceutical manufacturing operations, ensuring compliance with GMP and regulatory standards while driving safety, quality, and continuous improvement. Oversee production scheduling, KPIs, and cross-functional collaboration with engineering, quality, and supply chain teams. Implement Lean Manufacturing principles and operational efficiencies within a growing, regulated environment.

Smart4Sciences Nottingham, Nottinghamshire, United Kingdom

On-site Permanent