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 designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.

Johnson & Johnson MedTech

On-site Permanent

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing and implementing evaluation frameworks for generative AI agents used in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and partnering with AI engineering teams to improve AI applications in a regulated pharma environment.

Johnson & Johnson MedTech

On-site

Senior Specialist, Evidence Evaluation

In this role, you will create robust clinical evidence documentation to support the CE registration of medical devices, working closely with cross-functional teams to ensure product safety and performance. You will act as a subject matter expert, engaging in regulatory interactions and strategic business decisions.

Smith & Nephew Cannock Chase, United Kingdom

Hybrid Permanent

Site Director, Hull & Melton

Leads a strategically important manufacturing site for wound care products, driving long-term strategy, operational excellence, and large-scale transformation within a highly regulated environment. Champions cultural change, compliance, and innovation while leading cross-functional teams in manufacturing, quality, R&D, and regulatory. Plays a key role in global operations leadership, influencing supply chain strategy beyond the site.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Medical Devices Project Leader - Warwick

Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Drive project execution with a focus on high-volume manufacturability, particularly using injection-moulded plastics, while mentoring junior engineers and ensuring regulatory and design compliance. Play a key role in shaping technically robust, patient-focused medical technologies in a fast-paced environment.

Newton Colmore Warwick, United Kingdom

Hybrid Permanent

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

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

EHS Advisor

This role involves supporting the implementation and continuous improvement of an integrated Environmental, Health, and Safety (EHS) management system within a medical device manufacturing environment. The advisor will ensure compliance with UK regulations, lead sustainability initiatives, conduct audits, manage incident investigations, and deliver EHS training. Key responsibilities include maintaining risk assessments, safety procedures, and documentation while driving improvements in environmental performance and workplace safety.

Reading Industrial Pertemps Swindon, United Kingdom £42,000 – £47,000 pa

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

Quality Assurance Officer

This role involves maintaining and improving the Quality Management System (QMS) within a GMP-regulated pharmaceutical environment. The officer will lead internal audits, manage documentation, oversee regulatory compliance, and drive quality initiatives across manufacturing and supply chain operations. Key responsibilities include handling deviations, change controls, CAPAs, and supporting regulatory inspections and submissions.

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

On-site Permanent

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

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

Quality Manager

This role involves overseeing quality control processes on the manufacturing floor for electronic equipment, ensuring compliance with internal and regulatory standards. The Quality Manager will lead root-cause analysis, implement corrective actions, and work closely with engineering teams to transition products from prototype to production. Key responsibilities include maintaining SPC systems, driving continuous improvement, and ensuring adherence to ISO 9001 and IPC standards.

Advanced Technical Recruitment Nottingham, Nottinghamshire, 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