Latest Regulatory Affairs Jobs

Director Technology Leader Surgery - Germany & UK

This role involves shaping growth strategies, modernizing platforms, and delivering digital and AI capabilities for the Surgery business. The leader will partner with senior business leaders to develop technology as a competitive advantage, manage a regional technology budget, and ensure compliance with cybersecurity and regulatory requirements.

Johnson & Johnson MedTech

Director, Signal Detection Scientist

The Director, Signal Detection Scientist will lead the implementation of surveillance strategies for proactive detection and evaluation of new safety signals from post-marketing data. Responsibilities include developing and using novel tools and methodologies, performing signal validation, and communicating findings to safety management teams.

Johnson & Johnson MedTech

Preclinical In-Vitro Toxicology Scientist

This role involves leading and executing in-vitro toxicology studies, including Neutral Red, Ames, and micronucleus assays, within a regulated laboratory environment. The scientist will develop and optimise testing methodologies, interpret complex biological data, and support regulatory submissions. They will work collaboratively across multidisciplinary teams and with external partners to advance pre-clinical testing capabilities in product safety assessment.

Hudson Shribman United Kingdom £55,000 – £70,000 pa

Product Compliance Officer

The Product Compliance Officer will manage and advance product regulatory compliance for a healthcare technology company, focusing on infection prevention and control solutions. Key responsibilities include monitoring regulations, creating safety data sheets, and advising on product-related activities.

Hyper Recruitment Solutions Hertford, United Kingdom

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

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

Clinical Data & Systems Lead

This role involves leading complex clinical technology transformation and data migration initiatives across the clinical trial ecosystem. Responsibilities include managing end-to-end migration programmes, data validation, and ensuring compliance with regulatory requirements. The position requires strong clinical technology expertise and project management skills.

HAYS Specialist Recruitment Cambridge, United Kingdom £80,000 – £120,000 pa

PhD Studentship: Discovery of rational therapeutic biomarkers in breast cancer by systems pathology and deep learning

This PhD studentship involves using systems pathology and deep learning to discover therapeutic biomarkers in breast cancer. The project focuses on analyzing multimodal spatial datasets to understand tissue architecture and its impact on treatment efficacy, providing a unique opportunity to develop expertise in quantitative pathology and spatial cancer biology.

University of Cambridge Cambridge, South East England, United Kingdom

On-site Contract

Mechanical Engineer - Programme Manager - Drug Delivery Devices

This role involves leading multiple programmes focused on advancing next-generation drug delivery platforms, mentoring junior engineers, and taking ownership of core mechanical design activities. The position requires a strong background in mechanical engineering, experience with drug delivery devices, and the ability to balance technical innovation with commercial viability.

Newton Colmore Cambridge, United Kingdom

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

Director - Immunoassay Development

Leads the development of quantitative immunoassays from design through validation and commercialisation, with a focus on translating laboratory assays into point-of-care or microfluidic formats. The role involves hands-on science, team leadership, and collaboration with external advisors, within a regulatory-compliant environment. Requires deep expertise in immunoassay optimisation and experience with human biological samples.

Talentmark Stevenage, Hertfordshire, United Kingdom £75,000 – £100,000 pa

Clinical Advisor

The Clinical Advisor role at TPP involves providing expert advice and direction to support the development of SystmOne, representing the company at UK and international events, and ensuring compliance with healthcare standards. The role requires a broad knowledge of health and social care processes, clinical safety, and data protection, with a willingness to travel and work flexible hours.

TPP (The Phoenix Partnership) Horsforth, United Kingdom

Permanent

Complaints Data Analyst (Post Market)

This role involves leading monthly product quality monitoring, developing and maintaining Power BI dashboards, conducting complaint investigations, and supporting post-market surveillance activities. You will work closely with cross-functional teams to ensure regulatory compliance and drive continuous improvement in a global medical device company.

Carbon 60 London, United Kingdom £50 – £65 ph

Senior Clinical Study Startup Specialist

This role involves leading and accelerating clinical trial site activation across the UK, overseeing contracts and budgeting, and collaborating with R&D teams and NHS/site investigators. The position is based in Welwyn Garden City with a hybrid work pattern, requiring 2-3 days on-site.

Randstad Delivery Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £339 – £376 pd

Medical Software Safety Engineer

This role involves driving software safety activities for medical devices, conducting hazard analysis and risk assessments, and ensuring compliance with medical device standards. You will collaborate with cross-functional teams and support verification and validation processes.

Computer Futures London, City And County Of the City Of London, United Kingdom £75,000 – £85,000 pa