Latest regulatory affairs Jobs

Manager Medical Affairs International (m/f/d)

The Manager, Medical Affairs – International is a field-based role supporting the development of professional relationships with key opinion leaders in the therapeutic areas of Shockwave Medical. Responsibilities include providing scientific support, facilitating investigator-initiated studies, and collaborating with cross-functional teams to drive strategic initiatives and ensure compliance with regulations.

Johnson & Johnson MedTech Germany

Manager Medical Affairs International (m/f/d)

This role involves building professional relationships with key opinion leaders in the medical device industry, supporting investigator-initiated studies, and providing scientific expertise for Shockwave Medical products. The Manager will also collaborate with cross-functional teams to develop health economic insights and support internal training.

Johnson & Johnson MedTech

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

Sr. Director, Technology BU Interface – International (Orthopaedics)

This role involves leading the technology strategy and execution for DePuy Synthes' international operations, including Commercial, Supply Chain, Manufacturing, Quality, R&D, and enabling functions. The Sr. Director will act as a strategic partner to the President of International, managing technology demand, prioritization, and portfolio health, while ensuring secure, reliable, and scalable operations across EMEA, APAC, LATAM, Canada, and emerging markets.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Manager Ortho Supply Chain Procurement (SCP)

The Manager Ortho Supply Chain Procurement (SCP) role involves leading procurement activities for the Orthopaedics business, ensuring supplier performance, and aligning with business strategies. Key responsibilities include strategic sourcing, supplier management, and driving cost improvements. The role requires strong leadership, negotiation, and collaboration skills.

Johnson & Johnson MedTech

Manager Ortho Supply Chain Procurement (SCP)

The Manager Ortho Supply Chain Procurement (SCP) role involves leading procurement activities for the Orthopaedics business, ensuring supplier performance, and aligning procurement strategies with business needs. Key responsibilities include strategic sourcing, supplier management, and driving innovation in new product development.

Johnson & Johnson MedTech

Sr Principal Clinical Engineer

The Sr Principal Clinical Engineer acts as a Procedural Workflow Architect, defining end-to-end surgical workflows across preoperative, intraoperative, and postoperative care. This role translates clinical, usability, economic, and adoption needs into integrated procedural requirements that guide the development of implants, instruments, digital applications, and enabling technologies. The engineer collaborates with cross-functional teams to ensure solutions are intuitive, adoptable, and clinically differentiated.

Johnson & Johnson MedTech United States

On-site Permanent

Sr Principal Clinical Engineer

The role involves designing end-to-end surgical workflows across preoperative, intraoperative, and postoperative phases, translating clinical and operational needs into integrated procedural requirements. The engineer will collaborate with cross-functional teams to ensure medical solutions are intuitive, adoptable, and clinically meaningful, with a focus on innovation in orthopaedic treatments and digital surgery.

Johnson & Johnson MedTech £137,000 – £235,750 pa