This role involves managing clinical trial sites for Medtronic's Renal Denervation therapy, ensuring studies are conducted efficiently and in compliance with regulations. The specialist will build relationships with investigators, support data collection, and coordinate trial activities across Europe, with frequent travel required. The position supports transformative hypertension treatments within a global medical technology leader.
This role involves managing clinical trial sites and supporting Renal Denervation therapy studies within Medtronic's Interventional Cardiology Therapies team. The specialist ensures effective study execution by training site staff, maintaining regulatory compliance, and coordinating with cross-functional teams across Europe. It is a field-based, customer-facing position requiring extensive travel and strong communication with investigators and internal stakeholders.
The role involves providing expert clinical support and training to surgeons and theatre teams on innovative orthopaedic surgical technologies. The individual will manage high-value accounts, lead product trials, and support the adoption of medical devices in operating theatres. This field-based position requires strong clinical knowledge, relationship-building skills, and a commitment to improving patient outcomes through advanced surgical solutions.
This role involves leading technical strategy and project delivery for new product development in the medical device sector, with a focus on design control, regulatory compliance, and manufacturing process innovation. The individual will manage technical teams, ensure adherence to quality standards, and support the full product lifecycle from concept to commercialization within a regulated environment.
This role involves joining a two-year graduate programme at Johnson & Johnson MedTech in Leeds, focusing on the development and manufacturing of orthopaedic implants. You will work across R&D, Quality, Operations, and Manufacturing teams, gaining hands-on experience in product design, process development, and continuous improvement. The programme offers extensive training, mentorship, and opportunities for professional development.
This role involves leading commercial quality activities for Johnson & Johnson MedTech’s Surgery division in the UK and Ireland, ensuring compliance with medical device regulations and maintaining an effective Quality Management System (QMS). The specialist will manage non-conformances, CAPA investigations, audits, supplier approvals, and change controls while promoting a culture of quality and compliance. The position requires strong regulatory knowledge, collaboration across functions, and experience in highly regulated healthcare environments.
Technical Service Chemist required in Cheshire East, on a permanent basis. Requiring a degree or relevant qualification in Chemistry, Materials Science (or similar) and recent, proven industrial experience within laboratory testing, technical services, quality control or R&D. Candidates with coatings,...
New Product Development (NPD) Chemist required in Cheshire East, on a permanent basis. Requiring a degree in Chemistry, Materials Science (or similar) and recent, proven industrial experience of product development within a manufacturing environment. Candidates with coatings, adhesives, paper, film...
This role involves installing, commissioning, and maintaining a diverse range of medical equipment in healthcare environments. You will work independently, diagnose and solve technical issues, and build strong customer relationships through expert guidance and support.
This role involves leading the design and development of next-generation drug delivery devices, working closely with multidisciplinary teams to translate early-stage concepts into robust, manufacturable solutions. Responsibilities include hands-on involvement in concept generation, prototyping, and risk management, as well as mentoring junior colleagues and advising clients on technical decisions.
This role involves hands-on, multidisciplinary engineering to design and develop complex medical devices, working closely with a diverse team of specialists. The projects span multiple medical specialisms, including surgical robotics, but the role requires a broad interest in various device types and engineering challenges.
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.
This role involves ensuring quality and compliance across the full manufacturing lifecycle, from incoming materials to batch release, within a regulated environment. The Quality Engineer will maintain and improve the Quality Management System (QMS), lead root-cause analysis for non-conformances, support audits, and work closely with production and engineering teams to drive continuous improvement. The position is based in Rotherham and operates on a compressed workweek schedule.
This role involves leading quality improvement initiatives on the shop floor within a medical devices manufacturing environment. The engineer will conduct root-cause analyses, apply Continuous Improvement methodologies like DMAIC and 8D, and use statistical tools to reduce defects and enhance process capability. The position requires close collaboration with Production, Engineering, and Quality teams to ensure compliance with ISO 13485 and drive sustainable improvements in product and process performance.
This role involves servicing and repairing advanced medical systems and healthcare equipment. You will work with a global team of engineers, taking pride in your work and building long-term customer relationships. Opportunities for career progression into more technical roles are available.
