Jobs in Leeds

Embedded Software Engineer

This role involves designing and maintaining embedded C/C++ firmware for medical and mechatronic devices, taking full ownership of the software lifecycle, and establishing internal processes such as version control and documentation standards. The engineer will work hands-on with hardware teams, debug using test equipment, and lead the transition of firmware development from external contractors to in-house. It’s a rare opportunity to shape software engineering practices from the ground up within a small, mission-driven team focused on life-changing technology.

YT Technologies Belle Isle, West Yorkshire, WF1 5PS, United Kingdom £45,000 – £60,000 pa

Hybrid Permanent

Service Manager

Service ManagerOxford£60,000 - £75,000 Basic + Bonus + OEM Training + Stability + Work-Life Balance + Job Satisfaction + Appreciation + Family - Feel + Company Car (Personal Use) + Fuel Card + PensionTake the next step in your career...

Future Engineering Recruitment Ltd Oxford, Oxfordshire, United Kingdom £65,000 – £75,000 pa

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL

On-site Permanent

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Director, R&D Procurement (Antibody Drug Conjugates and Biopharmaceuticals)

Leads global procurement strategy for GSK's R&D in biopharmaceuticals and antibody drug conjugates, managing a £300M annual spend and a team of 4–6. Focuses on sourcing from CDMOs, negotiating complex contracts, and aligning supplier networks with R&D pipeline needs. Works closely with internal stakeholders and external partners to drive innovation, cost efficiency, and supply chain resilience.

GSK Stevenage, United Kingdom £108,000 – £180,000 pa

Hybrid Permanent

Director, Regulatory Affairs

Lead global regulatory strategy and execution for drug development programs, ensuring compliance across jurisdictions including the US, EU, and UK. Collaborate with cross-functional teams to prepare and manage regulatory submissions such as INDs, NDAs, and orphan drug designations. Provide strategic guidance on regulatory risks and lifecycle management, while engaging with health authorities and shaping regulatory science in the context of AI-driven drug discovery.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Fire Officer (on Shift)

We are looking to recruit a Shift Fire Officer to join our site team at our Montrose manufacturing site. The Shift Fire Officers advise on legal and other requirements affecting Environment, Health & Safety (EHS) at the site. Their purpose...

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

Head of Health Economics and Outcomes

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Manager, Global Regulatory Science CTA

Lead the end-to-end operational execution of Clinical Trial Applications (CTAs) outside the US, ensuring regulatory compliance and timely submissions across global markets. Serve as the subject matter expert on UK clinical trial regulations, including MHRA requirements and evolving legislation, while leveraging digital tools and AI-enabled technologies to enhance regulatory operations. Collaborate with cross-functional teams and CROs to maintain inspection-ready documentation and drive continuous improvement in regulatory processes.

Moderna Poland

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

Business Development Director

£75,000 - £80,000 per annum + 20% Bonus + Car AllowanceOffice is based in Hampshire, close to the Surrey borderFull Time | PermanentRegular UK Travel requiredOur client is an established international manufacturing and engineering business supplying innovative material solutions to...

HR Dept (Recruitment Agency) Farnborough, Hampshire, GU14 7JT, United Kingdom £75,000 – £80,000 pa

Audit Lead

Lead and develop GMP/GDP audit strategy for a key technology area such as sterile biologics or medical devices, ensuring compliance with global regulations and emerging trends. Conduct complex audits across Pfizer facilities, contract manufacturers, and suppliers, while coaching auditors and driving continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.

Pfizer London, SW7 2AP, United Kingdom £162,900 – £271,500 pa

Remote Permanent

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Audit Lead

Lead and develop GMP/GDP audit strategy for sterile biologics, medical devices, or small molecule manufacturing, ensuring compliance with global regulations and Pfizer standards. Conduct complex audits across internal sites and external partners, coach auditors, and drive continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.

Pfizer United States US$162,900 – US$271,500 pa

Remote Permanent