Latest regulatory affairs Jobs

Manager, EUDAMED & Data Transparency

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech Leeds, United Kingdom

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

Johnson & Johnson MedTech Leeds, 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

Optical Systems Engineer - Medical Devices - Cambridge

This role involves designing and integrating optical systems into complex medical technologies, from early feasibility to product launch. You will collaborate with a multidisciplinary team to develop devices that improve diagnostics, treatment, and patient outcomes, with a focus on precision, creativity, and regulatory compliance.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Mechanical Engineer - Programme Manager - Drug Delivery Devices

Mechanical Engineer - Programme Manager - Drug Delivery DevicesA period of significant growth has created an opportunity for a Programme Manager with a strong Mechanical Engineering background and deep, hands‑on experience in drug delivery device development. Based in Cambridge, you...

Newton Colmore Cambridge, United Kingdom

Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

Head of Product Development & Engineering

This role involves leading the product development lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, providing strategic direction, mentoring a specialist team, and collaborating with various departments to ensure product success and regulatory compliance.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 ph

Hybrid Contract

Design Engineer (Medical Devices / SolidWorks)

This role involves designing medical devices from concept to production, using SolidWorks to create 3D models and detailed drawings. The engineer will support prototyping, testing, and regulatory compliance while collaborating with manufacturing and cross-functional teams. The work contributes to life-changing healthcare products used globally.

Ernest Gordon Recruitment Lisburn, County Antrim, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

Quality Engineer

As a Q&RA Engineer, you will support quality and regulatory compliance across operations, working closely with cross-functional teams to maintain and improve quality systems. Key responsibilities include leading deviation investigations, managing change control, and supporting audits and inspections.

Hays Life Sciences Cheap, City And County Of the City Of London, United Kingdom

Hybrid Contract Flexible

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 Bolton, Manchester, M26 1HG, United Kingdom £40,000 – £50,000 pa

Quality Lead

This role involves leading quality and regulatory compliance for a multinational manufacturer across Europe and Africa, with a focus on medical devices and consumer products. The candidate will oversee the Quality Management System, lead audits, support new product launches, and drive continuous improvement through data analysis and cross-functional collaboration. It requires deep expertise in standards like MDD/MDR, ISO 13485, and QSR, along with strong leadership in technical quality environments.

New Appointments Group Folkestone, Kent, United Kingdom

On-site Permanent

Clinical Trials Associate

The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensure regulatory compliance, and support the delivery of clinical studies. Responsibilities include maintaining TMF, coordinating documentation, and assisting with site visits and data management.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff, requiring strong communication and technical skills.

Focus Resourcing United Kingdom

On-site Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a GMP-regulated pharmaceutical manufacturing environment. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams to ensure compliance and data integrity.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent