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

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

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

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, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management and supply chain operations across the UK, Canada, and Australia, aligning global strategies with local execution. Focuses on launch planning, supply chain resilience, cross-market coordination, and operational governance. Drives standardization, crisis preparedness, and continuous improvement through cross-functional leadership and digital transformation initiatives.

Moderna United States US$167,000 – US$300,700 pa

Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management, launch planning, and supply chain operations across the UK, Canada, and Australia, ensuring alignment between global strategy and local execution. Establishes governance, performance standards, and escalation frameworks while driving operational resilience, compliance, and cross-market collaboration. Focuses on S&OP, business continuity, crisis preparedness, and digital transformation through analytics and automation.

Moderna

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

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

Leads global procurement strategy for Antibody Drug Conjugates and Biopharmaceuticals, managing a £300M R&D spend and a team of 4–6. Focuses on sourcing from CDMOs, negotiating complex contracts, and aligning with GSK’s R&D pipeline acceleration. Works closely with internal stakeholders and external partners to drive value, cost control, and innovation in drug development.

GSK United States PLN 369,000 – PLN 615,000 pa

Hybrid 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

Senior Scientist (In vitro / Cellular Pharmacology), Cambridge, MA

This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.

Isomorphic Labs England

Hybrid Permanent