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, building benchmark datasets, and partnering with AI engineering teams to improve AI systems in specialized clinical contexts.

Johnson & Johnson MedTech Belgium
On-site Permanent

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing and implementing evaluation frameworks for generative AI agents used in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets to ensure AI systems meet the standards required by clinical and regulatory experts.

Johnson & Johnson MedTech
On-site Permanent
OrganOx logo

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom
On-site Permanent Flexible
Medtronic logo

Sales Representative

This role involves selling Medtronic's advanced medical devices, particularly Transcatheter Aortic Valves (TAVI) and Transcatheter Pulmonic Valves (TPV), to clinical and non-clinical stakeholders in the Midlands. Responsibilities include meeting sales targets, developing account plans, and providing technical support and training to hospital staff.

Medtronic Cambridge, United Kingdom £55,040 – £82,560 pa
On-site Permanent
Medtronic logo

Upstream Product Manager

The Upstream Product Manager will lead the strategy and early-stage development of AI-enabled and edge-based software solutions for the Touch Surgery ecosystem. Responsibilities include defining product vision, conducting market research, partnering with engineering teams, and developing go-to-market strategies. The role requires deep expertise in AI, edge computing, and software marketing.

Medtronic London, United Kingdom
On-site Permanent
OrganOx logo

Packaging Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom
On-site Permanent
Smith & Nephew logo

Marketing Manager (RENASYS)

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Are you driven by the opportunity to help shape global marketing strategy in a fast moving, innovation led environment? This is a chance to play a...

Smith & Nephew Watford, United Kingdom
Smith & Nephew logo

Surgical Training Technician

As a Surgical Training Technician, you will prepare and maintain laboratory spaces for surgical education, support live training sessions, and ensure compliance with regulatory frameworks. You will work closely with Medical Education, Marketing, and R&D teams, managing stock levels and maintaining inventory systems.

Smith & Nephew Watford, 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

Embedded Systems Engineer

This role involves developing and implementing embedded firmware solutions, designing and integrating electronic hardware, and working closely with cross-functional teams to bring next-generation scientific instruments to market. You will be part of a multidisciplinary R&D team, contributing to the entire product lifecycle from concept to production.

VRS UK Sheffield, South Yorkshire, United Kingdom £40,000 – £60,000 pa
On-site Permanent

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa
On-site Permanent

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa
On-site Permanent

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare and cleanroom environments. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Weston-super-Mare, Somerset, United Kingdom £35,000 – £40,000 pa
On-site Permanent

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare and pharmaceutical settings. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Stroud, Gloucestershire, United Kingdom £35,000 – £40,000 pa
On-site Permanent

Production Scheduler

As a Production Scheduler, you will plan and coordinate production activities for multiple projects in a low-volume, R&D-focused medical device manufacturing environment. You will ensure efficient resource allocation, timely delivery, and compliance with ISO13485 standards, acting as a key liaison between manufacturing, supply chain, quality, and engineering teams.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa
On-site Permanent