Latest Regulatory Affairs Specialist Jobs

Director, Regulatory Data Office Leader

The Director, Regulatory Data Office Leader, will lead a global team of data stewards and oversee the Regulatory Data Hub (RDH) to ensure high-quality regulatory data for business intelligence and decision-making. The role involves data governance, regulatory data stewardship, and collaboration with R&D, IT, and other departments to implement data standards and policies.

Johnson & Johnson MedTech

Director, Regulatory Data Office Leader

This role involves leading a global team of data stewards and overseeing the Regulatory Data Hub to ensure high-quality regulatory data for business intelligence and decision-making. The Director will establish data governance policies, collaborate across R&D and IT, and drive digital transformation initiatives.

Johnson & Johnson MedTech Belgium

Medical Sales Associate

Medical Sales AssociateCentral England & East Anglia (must live on patch - Oxon, Bucks, Beds, Herts, Cambs, Essex, Suffolk & Norfolk)£55,000–£65,000 OTE + benefitsWe’re recruiting a Medical Sales Associate for a well-established, quality-focused business supplying specialist products to hospitals and...

Parke Lane People Limited East Anglia, United Kingdom £55,000 – £65,000 pa

Senior NPI Engineer

Lead the quality aspects of new product introductions for complex electronic and medical devices, driving APQP/PPAP processes from design through to production. You'll manage FMEAs, control plans, and supplier compliance while ensuring regulatory standards are met. The role involves resolving early-stage quality issues, supporting audits, and improving product reliability in a regulated environment.

Jonathan Lee Recruitment Jersey Marine, West Glamorgan, SA10 6JJ, United Kingdom

Principal Scientist MSAT

Lead complex bioprocess transfer and scale-up projects into GMP manufacturing environments, ensuring robust, scalable processes. Drive technical delivery through experimental planning, data analysis, and cross-functional collaboration with operations, quality, and engineering teams. Support process investigations and regulatory compliance within a highly collaborative, multidisciplinary environment.

SRG Darlington, United Kingdom £49,045 – £65,045 pa

On-site Permanent

Product Manager

This Product Manager role involves end-to-end ownership of a healthcare product portfolio, driving growth through strategic planning, lifecycle management, and cross-functional collaboration. You'll shape market entry strategies, lead product launches, and translate customer insights into competitive advantages in the UK health sector. The role requires balancing regulatory, commercial, and technical demands while influencing global teams and supporting sales and marketing initiatives.

Drive Devilbiss Healthcare Halifax, West Yorkshire, HX1 1TH, United Kingdom

Lead Electronics Engineer

This role involves leading the design and development of medical-grade assistive technology devices that empower people with speech difficulties. Responsibilities include technical leadership, mentoring engineers, and collaborating across disciplines to ensure products are reliable, accessible, and innovative.

Smartbox Assistive Technology Bristol, United Kingdom

Equipment Maintenance & Facilities Engineer

This role involves maintaining and servicing laboratory, cleanroom, and production equipment in a regulated environment. Responsibilities include fault-finding, implementing corrective actions, and ensuring compliance with ISO 13485 standards. The position offers opportunities for continuous improvement and collaboration with R&D and Quality teams.

MP Recruitment Ox117Dt, United Kingdom

Product Manager

Product ManagerHalifaxProduct managementFull timePermanentWho We Are at Drive MedicalDrive Medical has become a leading manufacturer of medical products with a strong and consistent track record of growth achieved both organically and through acquisitions. We are proud of our high-quality, diverse...

Drive DeVilbiss Hx29Tn, United Kingdom

Site Director - Biologics CDMO

Lead a UK biologics manufacturing site within a global CDMO, overseeing end-to-end operations across manufacturing, quality, engineering, and supply chain. Ensure GMP compliance, drive operational excellence through Lean/Six Sigma, and lead regulatory engagements with MHRA, FDA, and EMA. Spearhead site strategy, capital projects, and client relationships in a regulated biopharmaceutical environment.

The Integrated Talent Partnership Cb10Ah, United Kingdom

Community IV Nurse

Are you a Registered Nurse with IV therapy experience looking for a role that offers autonomy, variety, and the opportunity to make a genuine difference?We're looking for aClinical IV Nurse to provide specialist care, education, and ongoing support to patients...

Inizio Cornwall, United Kingdom