Latest medical device engineer Jobs

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom

On-site Permanent Flexible

Packaging Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site Permanent

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will ensure compliance with UK MDR and EU MDR requirements, maintain technical documentation, and support regulatory submissions for Class I and Class IIa medical devices. You will work closely with the QA Manager to improve the Quality Management System and coordinate post-market surveillance activities.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Assembly Technician

Client;We are proud to be working alongside a truly ground-breaking medical device business, who are looking to appoint a process/assembly technician.POSITION; Process/Assembly TechnicianSHIFT; Monday - Friday 8 - 4:30Hourly Rate - £14.00 - £14.25 an hour.The key responsibilities for this...

Planet Recruitment Oxford, Oxfordshire, United Kingdom £14 – £14 ph

Senior Therapy Sales Specialist

This role involves working with the Acute Care & Monitoring (ACM) Team to drive sales and clinical education for Medtronic's Perioperative Complications product range in Scotland. Responsibilities include providing expert knowledge, building relationships with clinical stakeholders, and educating customers on the safe and effective use of Medtronic's products in operating rooms.

Medtronic Edinburgh, Alba / Scotland, United Kingdom £55,040 – £82,560 pa

On-site Permanent

District Sales Manager

The District Sales Manager will lead a sales team focused on promoting Medtronic's pain therapy solutions, including spinal cord stimulation and intrathecal drug delivery systems. Key responsibilities include building relationships with healthcare providers, fostering a high-performance sales culture, and collaborating with marketing and clinical teams to support product launches and physician education.

Medtronic London, United Kingdom £73,200 – £109,800 pa

On-site Permanent

Senior R&D Manager

As a Senior R&D Manager, you will lead the development of advanced wound care products, guiding scientific teams through the full lifecycle from concept to manufacture. Your role involves strategic direction, technical leadership, and ensuring regulatory compliance, while fostering innovation and high performance.

Smith & Nephew United Kingdom

Hybrid Permanent

QC Manager

Lead and manage the day-to-day operations of a QC laboratory within a regulated personal care and skincare manufacturing environment. Oversee analytical testing, root cause investigations, and ensure compliance with GMP, ISO, and GDP standards. Develop laboratory staff and drive continuous improvement in quality and performance.

SRG Po92Ax, PO9 2AX, United Kingdom

On-site Permanent

Operational Quality 1

The Operational Quality 1 role involves maintaining high standards of quality and compliance in the manufacturing process. Responsibilities include reviewing and releasing product documentation, managing non-conformances, and supporting quality audits. The role also involves leading investigations and dispositions of defective materials and ensuring compliance with quality management systems.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Technology Director, Make EMEA

This role leads the EMEA manufacturing technology strategy for DePuy Synthes, focusing on digital solutions like MES, automation, and data integration across regulated MedTech sites. The director partners with operations and quality leaders to ensure compliant, efficient, and standardized systems while leading regional teams and shaping global strategy. Key initiatives include digital manufacturing, cybersecurity, and data-driven decision-making in a highly regulated environment.

Johnson & Johnson MedTech Ireland

Hybrid Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote 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

Technical Specialist | J&J MedTech | Electrophysiology | East Midlands

The Technical Specialist role involves providing technical support for Electrophysiology (EP) procedures, promoting and upselling CARTO 3 procedures, and delivering customer training. The role also includes executing marketing strategies, maintaining relationships with key opinion leaders, and contributing to innovative activities to achieve sales targets.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid Permanent Flexible

Supplier Quality Engineer - Medical Devices - Oxford

The Supplier Quality Engineer will manage and develop the supplier base for a rapidly growing medical devices company, ensuring compliance with ISO 13485 standards. Responsibilities include evaluating suppliers, managing CAPAs, and applying quality expertise to design-for-manufacture considerations.

Newton Colmore Oxford, Oxfordshire, United Kingdom

On-site Permanent

Mechanical Engineer - Programme Manager - Drug Delivery Devices

Mechanical Engineer - Programme Manager - Drug Delivery DevicesA period of significant growth has created an opportunity for a Programme Manager with a strong Mechanical Engineering background and deep, hands‑on experience in drug delivery device development. Based in Cambridge, you...

Newton Colmore Cambridge, United Kingdom

Permanent