Latest regulatory affairs specialist Jobs

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing evaluation frameworks and rubrics for generative AI agents used in clinical operations and global development. Responsibilities include defining quality dimensions, designing human evaluation protocols, building benchmark datasets, and partnering with AI engineering teams to improve AI systems in specialized clinical contexts.

Johnson & Johnson MedTech

On-site

New Technology Specialist - Midlands - Johnson & Johnson MedTech | Electrophysiology

This role involves driving the adoption of new electrophysiology technologies in the Midlands region by providing expert clinical and technical support during product launches and in-field procedures. The specialist will lead training, design clinical evaluations, and act as a liaison between customers and internal teams to ensure successful implementation of new products like CARTO. A strong background in electrophysiology and a proven track record in field-based technical sales are essential.

Johnson & Johnson MedTech

Hybrid Permanent

Site Director, Hull & Melton

Lead and transform a strategically important manufacturing site within a highly regulated medical technology environment. Drive operational excellence across manufacturing, quality, regulatory, R&D, and finance functions while fostering a culture of innovation and continuous improvement. Serve as a key member of the global operations leadership team, influencing broader supply chain strategy and large-scale transformation initiatives.

Smith & Nephew Melton, United Kingdom

On-site Permanent

Senior Manufacturing Engineer - CMO

As a Senior Manufacturing Engineer - CMO, you will lead strategic initiatives and projects to enhance the Advanced Wound Management portfolio. You will manage complex changes, collaborate with cross-functional teams and external partners, and ensure regulatory compliance and quality. The role involves developing and implementing key projects to drive product sustainment and value creation, while also providing engineering support to key suppliers and maintaining manufacturing resilience.

Smith & Nephew United Kingdom

Hybrid Permanent

Production Assembler (Medical Devices)

This role involves assembling electro-mechanical micro-components for implantable medical devices in a cleanroom environment, with strict adherence to quality and regulatory standards. The Production Assembler will perform precision assembly, in-process inspections, and maintain accurate documentation as part of a small, dedicated team. It offers hands-on work in a regulated, high-precision setting with direct impact on patient outcomes.

Amber Therapuetics Oxfordshire, United Kingdom £30,000 pa

On-site Permanent

Quality Assurance Officer

This role involves maintaining and improving a Quality Management System (QMS) in a pharmaceutical GMP-regulated environment. The individual will lead internal audits, manage documentation, oversee deviations and change controls, support regulatory inspections, and ensure compliance with MHRA, GMP, and ISO standards across manufacturing and supplier operations.

Reed Al40Jy, AL4 0JY, United Kingdom £28,000 – £32,000 pa

On-site Permanent

Senior Director, Product Management - Sequencing Systems

The Senior Director of Product Management will lead the strategy and lifecycle management of sequencing systems, working closely with R&D, Product Development, Commercial, Marketing, Operations, and Regulatory teams to ensure products deliver customer value and align with company strategy.

Oxford Nanopore Technologies Oxford, United Kingdom

On-site Permanent

Quality Engineer, Medical Devices

Quality Engineer, Medical DevicesBasic Salary £40,000 to £50,000HealthcarePensionThe Role - Quality Engineer, Medical DevicesFollowing expansion, they seek to recruit a Quality Engineer responsible for all aspects of quality management including:Drafting processes, procedures and documentationPerforming internal auditsManaging and resolving complaintsYour Background...

TRS Consulting Preston, East Riding of Yorkshire, HU12 8SB, United Kingdom

Principal Clinical Research Specialist

The Principal Clinical Research Specialist will lead and manage multi-site clinical studies for Pelvic Health across Europe, ensuring compliance with regulations and delivering high-quality clinical evidence. Responsibilities include designing study protocols, overseeing trial operations, and collaborating with investigators and cross-functional teams.

Medtronic Watford, United Kingdom £64,800 – £97,200 pa

Remote Permanent

Quality Engineer, Validation

This role involves leading process and test method validation for medical device manufacturing, focusing on injection moulding, assembly, sterilisation, and packaging. The engineer ensures validation strategies align with ISO 13485 and ISO 14971, supports design transfer, and provides quality oversight at supplier sites. Key responsibilities include developing validation plans, executing IQ/OQ/PQ, performing MSA, and delivering audit-ready documentation.

OrganOx Oxford, United Kingdom

On-site Permanent

Principal Embedded Software Engineer - 6-Month

As a Principal Embedded Engineer, you will work on expanding the feature set of existing medical devices and ensuring the codebase is maintainable. You will collaborate with multidisciplinary teams to develop and productize custom computing devices, optimize performance, and ensure robust and secure software for medical-grade systems.

Medtronic London, United Kingdom

On-site Contract

Sales and Applications Specialist - Mobile Surgery

This role involves promoting mobile surgery products, providing technical expertise during sales presentations and demonstrations, and supporting account managers in achieving business growth. The candidate will also train customers, maintain customer relationships, and stay updated on product developments and compliance standards.

Philips United Kingdom

Remote Permanent

Full Stack Developer

The Full Stack Developer role involves hands-on software engineering, focusing on building and maintaining high-quality applications and solutions across OrganOx's digital platforms. Responsibilities include coding, API design, database management, DevOps, and collaboration with internal and external teams to support regulated medical device and data solutions.

OrganOx Oxford, United Kingdom

On-site Permanent

Field Service Engineer

This role involves providing technical support and maintenance for Philips Imaging's advanced healthcare equipment, including installation, repair, and preventive maintenance. The Field Service Engineer will work in a 5x7 rotation, supporting customers remotely and on-site, and must be based in the Newcastle, Durham, or Darlington area.

Philips United Kingdom

Remote Permanent Flexible 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