Latest regulatory affairs specialist 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

On-site Permanent

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 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

Laboratory Analyst 2

This role involves performing analytical testing of raw materials, intermediates, and finished medical products using techniques like ICP, GC, IR, UV-Vis, and TOC. The Laboratory Analyst 2 supports quality assurance by maintaining methods, investigating out-of-specification results, validating processes, and ensuring compliance with safety and regulatory standards. The position also includes mentoring junior staff, driving continuous improvement, and contributing to method development and equipment validation.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

QMS Specialist

As a QMS Specialist, you will ensure the Quality Management System meets global medical device regulations, support key QMS processes, and collaborate with cross-functional teams to maintain audit readiness. Your role involves interpreting regulatory requirements, conducting data analysis, and driving continuous improvement to ensure high-quality, compliant products.

Smith & Nephew Goole, 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

Senior QA Validation Engineer

This role involves leading software verification and validation for safety-critical systems in a regulated environment, with a focus on test automation, regulatory compliance, and end-to-end traceability. The engineer will design test strategies, develop automated frameworks, and ensure alignment with quality standards across the development lifecycle. Collaboration with cross-functional teams is essential to resolve quality issues and support audits or regulatory submissions.

SoCode Impington, Cambridgeshire, United Kingdom £80,000 – £100,000 pa

On-site Permanent

Operations Manager

This role involves leading daily operations at a GMP-regulated manufacturing and distribution facility, ensuring compliance, safety, and efficiency across production, quality, and technical teams. The Operations Manager will drive performance, lead investigations into deviations, manage site KPIs, and support continuous improvement initiatives. It is a hands-on leadership position with significant responsibility for regulatory readiness, team development, and operational excellence.

SKC Recruitment Chilwell, Nottinghamshire, NG9 5FZ, United Kingdom £50,000 – £55,000 pa

On-site Permanent

Junior AI Healthcare Specialist

Position SummaryWe are seeking motivated and innovative Junior Healthcare AI Specialists to join our team and contribute to the development of advanced artificial intelligence solutions that support healthcare professionals, improve patient outcomes, and enhance operational efficiency across healthcare environments. This...

Global Tech Recruitment London, United Kingdom £38,000 – £40,000 pa

Software Lead

This role involves leading software development for wearable medical devices, from early R&D through to commercial release, with a focus on regulatory compliance and cross-functional collaboration. The Software Lead will define technical strategy, contribute hands-on to architecture and problem-solving, and coordinate multidisciplinary teams including internal developers and external partners. It's a foundational role shaping the software platform for future product expansion in a regulated medical technology environment.

Cure Talent Loughborough, Leicestershire, LE11 2QG, United Kingdom £75,000 – £90,000 pa

Hybrid Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract

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

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

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