Latest regulatory affairs Jobs

Director, Regulatory Data Office Leader

The Director, Regulatory Data Office Leader, will lead a global team of data stewards and oversee the Regulatory Data Hub (RDH) to ensure high-quality regulatory data for business intelligence and decision-making. Key responsibilities include data governance, regulatory data council leadership, and transformation enablement through digital solutions and AI.

Johnson & Johnson MedTech United States £150,000 – £258,750 pa

Director, Regulatory Data Office Leader

This role involves leading a global team of data stewards and overseeing the Regulatory Data Hub to ensure high-quality regulatory data for business intelligence and decision-making. The Director will establish data governance policies, standards, and collaborate across R&D, IT, and data science to drive regulatory data excellence and transformation initiatives.

Johnson & Johnson MedTech £150,000 – £258,750 pa

Principal Market Development and Strategic Marketing Specialist

Lead market development for cardiac conduction system pacing and bradycardia/CRT-P therapies across Western Europe, translating clinical evidence into actionable strategies and customer tools. Drive product launches, adoption, and cross-functional alignment with country teams, sales, and clinical stakeholders. Focus on removing clinical, operational, and perception barriers to therapy uptake through scalable frameworks and customer-centric execution.

Medtronic

Principal Market Development and Strategic Marketing Specialist

This role involves leading market development and strategic marketing for cardiac conduction system pacing and bradycardia/CRT-P therapies across Western Europe. The specialist will drive therapy adoption, launch execution, and translate clinical evidence into actionable tools and value narratives. Collaboration with cross-functional teams and country marketing units is central to removing adoption barriers and scaling regional growth.

Medtronic €53,600 – €80,400 pa

Senior Development Technologist

This role involves leading technical strategy and project delivery for new product development in the medical device sector, with a focus on design control, regulatory compliance, and manufacturing process innovation. The individual will manage technical teams, ensure adherence to quality standards, and support the full product lifecycle from concept to commercialization within a regulated environment.

Smith & Nephew United Kingdom

Medical Devices Project Leader - Warwick

Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Drive project execution with a focus on high-volume manufacturability, particularly using injection-moulded plastics, while mentoring junior engineers and ensuring regulatory and design compliance. Play a key role in shaping technically robust, patient-focused medical technologies in a fast-paced environment.

Newton Colmore Warwick, United Kingdom

Hybrid Permanent

Mechanical Design Engineer

Design and develop complex injection moulded plastic components and polymer-based medical devices, focusing on scalability, manufacturability, and regulatory compliance. Lead concept-to-production design projects involving robotics and mechatronics, working closely with manufacturing partners and cross-functional teams. Engage in hands-on prototyping, materials selection, and design validation within a regulated medtech environment.

Innovo Global Talent Warrington, Cheshire, United Kingdom £35,000 – £45,000 pa

Medical Systems Engineer

This role involves capturing and managing requirements for medical devices, ensuring compliance with regulatory standards in both hardware and software engineering. The engineer will design and implement development processes, with a focus on best coding practices and test procedures. Work is primarily remote, with occasional travel to Cheltenham.

Circuit32 Recruitment Cheltenham, Gloucestershire, United Kingdom £50 – £65 ph

Remote Contract

Scientist

The Scientist role involves hands-on R&D support for new product development, line extensions, and design changes, focusing on sterile, single-use medical devices. Responsibilities include laboratory testing, verification, validation, and maintaining regulatory documentation.

Cure Talent Crewe, Cheshire, United Kingdom £28,000 – £34,000 pa

On-site Temporary

Quality Assurance Manager, Medical Device & Combination Products

This role involves providing quality oversight for medical device and combination product programs across development and sustaining phases. The individual will lead complaint investigations, ensure compliance with design controls and regulatory standards, and support cross-functional teams in risk-based decision-making. Focus areas include change management, post-market surveillance, and continuous improvement of quality systems in a highly regulated environment.

Pfizer Cambridge, Cambridgeshire, United Kingdom

Technical Writer

Produces and maintains technical documentation for sequencing devices, ensuring accuracy, regulatory compliance, and clarity for customers and external bodies. Works within a quality-managed environment to support product releases and safety standards. Translates complex technical and scientific information into accessible content.

Oxford Nanopore Technologies Oxford, United Kingdom

Senior Product Development Scientist

Leads product development projects in the medical devices sector, focusing on assay development, optimisation, and lifecycle management within regulated environments. Responsible for data analysis, regulatory compliance, equipment validation, and mentoring junior staff. Works in a collaborative, innovation-driven setting with a strong emphasis on quality and continuous improvement.

STEM Recruitment Queen Street, Edinburgh, United Kingdom

Service Engineer

This role involves maintaining and repairing medical decontamination equipment, including sterilizers, washer disinfectors, and endoscopes. The engineer will perform diagnostic repairs on electrical, mechanical, pneumatic, and plumbing systems across healthcare facilities. The position requires strong technical troubleshooting, regulatory compliance awareness, and independent fieldwork across the Bristol region.

Ascend Consulting Bristol, Bristol (county), United Kingdom £35,000 – £48,000 pa

Compliance Officer

This role involves leading product regulatory compliance for a portfolio of chemical and healthcare products, with responsibilities including monitoring regulations, preparing Safety Data Sheets, and supporting product registrations in the UK and Europe. The Compliance Officer will act as the main contact for external regulators, deliver internal training, and ensure compliance across product development and marketing. The position requires a scientific background and experience with chemical regulations such as REACH and CLP.

Reed Sg12Fs, United Kingdom £45,000 – £55,000 pa

Hybrid Permanent

Senior Quality Engineer

This role involves owning and improving the Quality Management System (QMS) within a medical device manufacturer, ensuring compliance with ISO 13485, EU MDR, and FDA regulations. The engineer will lead QMS processes including deviation management, CAPA, document control, and internal audits, while collaborating with operations, regulatory, and supply chain teams. Key responsibilities include supplier audits, root cause analysis, and driving continuous quality improvements in a highly regulated environment.

Walker Cole International Leeds, West Yorkshire, United Kingdom