Latest Regulatory Affairs Specialist Jobs

Senior Field Clinical Research Specialist

This role involves managing clinical trial sites and providing on-site support for Renal Denervation therapy studies within Medtronic’s Interventional Cardiology Therapies team. The specialist ensures high-quality data collection, supports case enrollment, and maintains compliance with regulations while building relationships with investigators and cross-functional teams. The position operates remotely across several European countries with extensive travel required.

Medtronic £50,400 – £75,600 pa

Electronics Engineer Consultant - Security Clearance

Electronics Engineer Consultant - Security Clearance - CambridgeA new design consultancy, based in Cambridge, are currently looking for a Electronics Engineer Consultant to add to the team of experienced experts, specifically with a focus on security cleared projects.Although this is...

Newton Colmore Cambridge, United Kingdom

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 customer-facing tools and driving adoption through cross-functional collaboration. Focus on launch execution, barrier removal, and strategy alignment with regional teams. Role involves 20-35% travel across the region.

Medtronic Spain

Medical Safety Officer - PALM

This role involves leading the medical safety assessment of pharmaceutical products in clinical development and post-approval, with a focus on signal detection, risk management, and regulatory compliance. The Medical Safety Officer provides strategic medical input into safety documentation, collaborates across clinical and regulatory teams, and ensures accurate communication of safety data to internal stakeholders and health authorities. The position plays a key role in shaping risk mitigation strategies and maintaining compliance with global pharmacovigilance standards.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Medical Safety Officer - PALM

This role involves leading the safety assessment and risk management of pharmaceutical products across their lifecycle, with a focus on evaluating safety data from clinical trials and real-world sources. The Medical Safety Officer provides strategic medical oversight to cross-functional teams, contributes to regulatory submissions, and ensures compliance with global pharmacovigilance standards. Key responsibilities include leading Safety Management Teams, developing risk mitigation strategies, and communicating safety findings to internal leadership and health authorities.

Johnson & Johnson MedTech

Senior Director, Site Lead - Hull & Melton

Lead a strategically important manufacturing site within a global medical technology organization, driving long-term strategy, operational excellence, and large-scale transformation across manufacturing, quality, R&D, and regulatory functions. Champion a culture of innovation, compliance, and continuous improvement in a highly regulated environment. Play a key role in the global operations leadership team, influencing broader supply chain strategy while developing a high-performing, multi-functional leadership team.

Smith & Nephew Melton, United Kingdom

On-site Permanent

Site Director, Hull & Melton

Lead a strategically important manufacturing site within a global medical technology company, driving long-term strategy, operational excellence, and large-scale transformation across multi-functional teams. Champion a culture of innovation, compliance, and continuous improvement in a highly regulated environment. Play a key role in the global operations leadership team, influencing broader supply chain strategy while ensuring performance, safety, and regulatory standards are consistently met.

Smith & Nephew Goole, 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

Quality Engineer

As a Quality Engineer, you will drive quality excellence in a regulated manufacturing environment, leading improvement initiatives, compliance efforts, and problem-solving. You will collaborate with cross-functional teams to ensure product quality, process performance, and regulatory compliance, using structured methodologies and statistical analysis.

Consortium Professional Recruitment Hessle, East Riding Of Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Senior Design Assurance Engineer

This role involves ensuring medical device designs comply with global regulatory standards throughout the product development lifecycle. You'll lead design assurance activities including risk management, design controls, and verification/validation, working closely with engineering and quality teams. The position emphasizes compliance with ISO 13485, ISO 14971, and 21 CFR Part 820 within a highly regulated environment.

SRG Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

Clinical Advisor

The RoleTPP are expanding their clinical team and are seeking a clinical advisor to support the ongoing development of SystmOne.TPP’s world-class technology supports professionals across all areas of the NHS health and social care system, as well as providers in...

TPP (The Phoenix Partnership) Horsforth, United Kingdom

Permanent

Manufacturing Engineer

This role involves designing and optimizing manufacturing processes for medical devices, with a focus on instrumentation and electromechanical systems. The engineer will lead process improvements, support verification and validation at contract manufacturing organizations (CMOs), and ensure compliance with quality standards. Key responsibilities include driving design for manufacturability, managing technical projects, and maintaining rigorous documentation within a regulated environment.

GxPeople Global Trowbridge, Wiltshire, BA14 8EY, United Kingdom £55,000 – £65,000 pa

Field Service Manager

The Field Service Manager will act as a technical expert for complex product issues in a global healthcare robotics environment. This role involves root cause analysis, creating diagnostic procedures, and bridging field service with engineering and quality teams. The position drives product reliability improvements and supports regulatory compliance within a highly regulated, innovative technology setting.

AES Impington, Cambridgeshire, United Kingdom £40,000 – £50,000 pa

Senior Quality Associate

This role involves overseeing key quality assurance processes such as NCR, CAPA, and change control within a medical device development environment. The individual will ensure compliance with regulatory standards, support audit readiness, lead training initiatives, and drive continuous improvement across QA systems. Emphasis is placed on data integrity, cross-functional collaboration, and maintaining robust documentation for design history and regulatory submissions.

Adepto Technical Recruitment Ltd Cambridge, Cambridgeshire, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving quality management systems for medical software and hardware products, with responsibilities including managing nonconformances, CAPA, change control, internal audits, and SOPs. The specialist will identify process gaps, enhance compliance, and support regulatory documentation within a fast-growing healthcare tech environment. The position requires a hands-on approach to streamline quality workflows and reduce backlogs in an evolving QMS.

Cure Talent London, United Kingdom £55,000 – £65,000 pa