Latest regulatory affairs Jobs

Director, MedTech Surgery Data Analytics & AI

This role involves leading the data strategy, analytics, and AI initiatives for MedTech Surgery at Johnson & Johnson. The Director will build and manage a team focused on developing trusted, compliant, and scalable data products that enhance decision-making and innovation across various domains, including R&D, commercial, supply chain, and digital surgery. The position requires deep collaboration with business stakeholders to ensure value realization and compliance.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Principal Portfolio Lead Clin Prog

This role involves formulating and executing the clinical programming strategy for a portfolio of medium to high complexity clinical trials. Responsibilities include planning, resource allocation, cross-functional collaboration, and ensuring compliance with quality and regulatory standards.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent
Newton Colmore logo

Medical Devices Project Leader - Cambridge

Medical Devices Project Leader - CambridgeWe are seeking a dynamic and driven Project Leader to join our innovative medical devices team based in Cambridge. This is a unique opportunity to lead cutting-edge development projects that directly impact patient care and...

Newton Colmore Cambridge, United Kingdom
Permanent

Junior Biomedical Field Engineer

The Junior Biomedical Field Engineer will perform preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will support the site manager, maintain service documentation, and interact with customers and OEM staff, while adhering to safety and regulatory standards.

Focus Resourcing United Kingdom
On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving the company's Quality Management System (QMS) within a regulated Medical Device manufacturing environment. Responsibilities include ISO13485 compliance, internal auditing, CAPA management, complaint investigations, and regulatory support. The position is office-based and requires strong documentation and procedural writing skills.

East Lancashire Services Crimble, Manchester, OL11 4AB, United Kingdom
On-site Permanent

QC Analyst

This role involves hands-on analytical testing of raw materials, intermediates, and finished products within a GMP-regulated laboratory. The QC Analyst ensures data integrity in line with ALCOA+ principles, investigates deviations and non-conformances, and maintains strict compliance with quality, safety, and documentation standards. The position supports continuous improvement initiatives in a quality-focused scientific environment.

Smart4Sciences Netherlands, United Kingdom
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
Medtronic logo

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
OrganOx logo

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
Medtronic logo

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
Philips logo

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
OrganOx logo

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
Smith & Nephew logo

Senior Counsel, Global R&D Commercial

This role involves providing strategic legal advice to R&D, IP, and commercial teams, drafting and negotiating complex agreements, and supporting product development and commercialization. The position plays a key role in managing legal risks and enabling business opportunities across global markets.

Smith & Nephew Watford, United Kingdom
Hybrid Permanent
Smith & Nephew logo

Quality Engineer

As a Quality Engineer, you will lead quality initiatives in a manufacturing environment, ensuring the reliability and compliance of medical devices. You will apply statistical process control, conduct root cause analysis, and collaborate with cross-functional teams to drive continuous improvement and maintain quality standards.

Smith & Nephew Goole, United Kingdom
On-site Permanent
Philips logo

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