Latest regulatory affairs specialist Jobs

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, working with a high level of independence to ensure timely and scientifically sound document delivery.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading team projects, and guiding cross-functional team members on processes and best practices. The position focuses on the Immunology therapeutic area and supports the development of transformational medicines for immunological disorders.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Director, Procurement Technology & Enablement

Leads the end-to-end procurement technology strategy and digital transformation for a global, regulated enterprise, focusing on building a modern, data-driven Source-to-Pay (S2P) ecosystem. Drives platform governance, data analytics, process simplification, and change management to improve compliance, user experience, and business outcomes across procurement. Works cross-functionally with IT, Finance, Legal, and procurement teams to deliver scalable solutions and embed digital capabilities.

Smith & Nephew Cannock Chase, United Kingdom US$220,000 – US$240,000 pa

On-site Permanent

Director, Procurement Technology & Enablement

Lead the strategy and delivery of a global, data-driven Source-to-Pay (S2P) ecosystem, owning the technology roadmap, data governance, and digital transformation across procurement. Drive adoption, change management, and analytics capabilities while partnering with IT, Finance, and business leaders to enable measurable business outcomes in a regulated, global environment.

Smith & Nephew United States US$220,000 – US$240,000 pa

On-site Permanent

Technical Consultant - Spine

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...

Medtronic United Kingdom £42,000 – £63,000 pa

On-site Permanent Flexible

Therapy Development Specialist

This role involves driving sales and market share for Transcatheter Aortic Valves (TAVI) and Transcatheter Pulmonic Valves (TPV) in the Midlands. Responsibilities include developing therapy plans, engaging key stakeholders, and providing technical support and training to hospital staff.

Medtronic United Kingdom £53,600 – £80,400 pa

On-site Permanent

Mechanical Design Engineer, Consumables

The Mechanical Design Engineer, Consumables role involves hands-on design, development, and verification of next-generation class III consumable perfusion sets. You will work within a cross-functional R&D team, collaborating with internal and external stakeholders to ensure high-quality product delivery and compliance with regulatory standards.

OrganOx Oxford, United Kingdom

On-site Permanent

Electronics Design Engineer

The Electronics Design Engineer will design, develop, and support electronics systems for OrganOx’s medical devices, ensuring compliance with regulatory and safety standards. Responsibilities include full lifecycle electronics design, from concept to manufacturing, with a focus on reliability, safety, and manufacturability.

OrganOx Oxford, United Kingdom

On-site Permanent

Clinical Application Specialist (Monitoring Analytics) - North of England

This role involves promoting Philips Healthcare products and providing comprehensive training to customers across the North of England. You will work closely with account and product managers to ensure optimal use of equipment, support new product launches, and maintain high customer satisfaction.

Philips United Kingdom

Remote Permanent Clearance Required

Validation Specialist

The Validation Specialist role involves enhancing validation practices, supporting compliance with regulatory inspections, and streamlining processes. You will identify risk areas and implement mitigation strategies to meet standards set by bodies like the MHRA and FDA.

Norgine Hengoed, CF82 7NL, United Kingdom

On-site Contract

Regional CHC Operations Coordinator

Want a 3D Career? Join Norgine.At Norgine, our colleaguesDare themselves to be different and try new things,Drive to achieve their goals and beyond, andDevelop themselves and their community.We call it the3D career at Norgine and it offers you a fully-rounded...

Norgine Uxbridge, UB8 1SB, United Kingdom

Hybrid

Clinical Trial Coordinator

The Clinical Trials Coordinator will work closely with a renowned professor and the Lead Clinical Trials Coordinator to manage and coordinate multiple research trials and projects. Responsibilities include data collection, regulatory compliance, patient communication, and assisting with the publication of academic papers, with a focus on advanced diagnostic and treatment methods in medical retina and vitreoretinal conditions.

IDA Recruitment Ltd Cavendish Square, London, United Kingdom £28,000 – £45,000 pa

On-site Permanent

PhD Level Ultrasound Technology Consultant - Cambridge

This role involves driving the development of next-generation surgical and interventional devices using advanced ultrasound technology. Responsibilities include leading high-impact technical programmes, collaborating with partner organisations, and applying scientific expertise from feasibility studies to market preparation.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

This role involves leading the design and development of next-generation drug delivery devices, working closely with multidisciplinary teams to translate early-stage concepts into robust, manufacturable solutions. Responsibilities include hands-on involvement in concept generation, prototyping, and risk management, as well as mentoring junior colleagues and advising clients on technical decisions.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Design Engineer - Medical Devices

This role involves designing and developing components for medical devices, supporting new product development, and conducting verification and validation activities. You will work on cutting-edge technologies like electromechanical systems and connected devices, collaborating with cross-functional teams and ensuring compliance with medical device standards.

Gold Group Falmouth, Cornwall, United Kingdom £45,000 pa

On-site Permanent