Latest regulatory affairs Jobs

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Export Control Analyst

The Export Control Analyst role involves supporting global trade compliance activities, ensuring products and data are exported in line with export control laws. Responsibilities include screening, classification, and transaction reviews, maintaining records, and providing guidance to various teams.

Johnson & Johnson MedTech Leeds, United Kingdom

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

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 Development Specialist

This role involves leading the launch and adoption of the Affera Mapping System and Cardiac Ablation Solutions (CAS) portfolio. Responsibilities include site initiations, providing clinical and technical expertise, training clinicians, and ensuring regulatory compliance. The role requires a strong background in electrophysiology and ablation technologies, with a focus on 3D mapping systems and complex EP procedures.

Medtronic Watford, United Kingdom

On-site Permanent

R&D Engineer

As an R&D Engineer, you will work within a collaborative team to develop the next generation of medical devices, from early concept to clinical trials and manufacturing. Your role involves planning and delivering engineering work packages, translating user needs into engineering requirements, and working closely with cross-functional teams to ensure robust design outputs and regulatory compliance.

Smith & Nephew United Kingdom

Hybrid Permanent

Staff Systems Verification Engineer: Digital Projects

The Staff Systems Verification Engineer will lead the development and execution of test strategies for digital and electromechanical medical devices, ensuring compliance with regulatory standards. They will work closely with cross-functional teams to create and maintain test environments, including automation, and improve team productivity.

Smith & Nephew 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

Senior Analyst

The Senior Analyst role involves developing and refining pharmaceutical business fundamentals databases, supporting product and client needs, and collaborating with local and offshore teams. Responsibilities include data collection, quality control, and enhancing database accuracy and scope.

GlobalData Plc Blackfriars, City And County Of the City Of London, EC4V 6BJ, United Kingdom

Hybrid Permanent

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