Medical Technology Jobs

Johnson & Johnson MedTech · Raritan, United States · US$102,000 – US$177,100 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors performing anonymisation and synthetisation, serves as the primary contact for YODA Project requests, and supports external research teams using clinical study data. Operates independently as a subject matter expert within the Clinical Data Standards and Transparency team.

Johnson & Johnson MedTech · High Wycombe

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.

Smith & Nephew · Wrocław, Poland

Acts as a trusted advisor to Finance and Global Business Services teams, translating strategy into technology-enabled change and building business cases through governance. Manages the ERP enhancement pipeline and stays close to delivery, ensuring solutions meet business needs. Requires deep SAP ECC and S/4HANA FICO functional knowledge across complex change programmes.

Smith & Nephew · Hull

Leads strategic initiatives to shape and continuously improve a global compliance programme, simplifying processes, enhancing systems and overseeing reporting, communications and training roadmaps. Works cross-functionally with Compliance, Finance and People teams, measuring programme effectiveness and supporting leadership reporting.

GE HealthCare · Chalfont Saint Giles

Leads global strategic sourcing and procurement for external manufacturing (CMO) services, covering finished goods, sub-assemblies and specialised components. Drives complex supplier negotiations, market and risk analysis, supplier performance management and contract lifecycle compliance, working cross-functionally with R&D, Engineering, Quality, Supply Chain, Finance and Operations. Hybrid role with global travel.

Medtronic · London · £87,600 – £131,400 pa

Owns the multi-year product vision and platform strategy for an edge-compute and connectivity foundation used in operating rooms, spanning video, data movement, fleet operations and real-time AI workloads. Works with engineering, clinical and commercial partners in a regulated environment, requiring at least two days a week in the London office.

University of Leeds · Leeds · £41,064 – £48,822 pa

Develop a clinically deployable assay for therapeutic drug monitoring of the immunosuppressant tacrolimus, building on a recently created rapid, accurate and low-cost measurement method. Work within a multidisciplinary team focused on in vitro diagnostics assays and devices that improve dosing and patient outcomes, replacing slow mass spectroscopy workflows.

Newton Colmore · Cambridge

Provide regulatory support across a product development organisation, working with engineers and scientists to align projects with global requirements. Maintain and improve the QMS, apply ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, and support external audits.

Pertemps Gloucester · Cheltenham · £25,000 – £27,000 pa

Assembling precision medical devices within a controlled cleanroom, working to GMP standards and ISO procedures to meet production targets. The role involves handling small components with high accuracy in a fast-paced, high-volume environment, with full training provided. It offers a four-day week, Monday to Thursday, with Fridays off.

ACS Staffing Solutions · Malvern · £40,000 – £50,000 pa

Lead the Service and Repairs function for an assistive technology company, combining hands-on electronic fault diagnosis with team leadership and operational improvement. You'll coach technicians, drive root cause investigations with Hardware Engineering, and improve turnaround times and processes while preparing the department for ISO 13485 compliance. The role sits at the intersection of accessibility, technical troubleshooting and quality/regulatory work.

Omega Resource Group · Gloucester · £45,000 – £50,000 pa

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.

Carbometrics · Bristol · £60,000 – £70,000 pa

Lead the development of a signal-processing pipeline that turns raw optical sensor measurements into reliable analytical results, covering filtering, noise removal, bias compensation, calibration and change detection. Work hands-on with experimental data in Python, building algorithms and visualisation tools alongside scientists and engineers, with scope to grow into a team-leading role.

Medtronic · Warsaw, Poland · PLN 88,000 – PLN 132,000 pa

Primary point of contact for customers through the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.

ProTech Recruitment Ltd · Dorking · £45,000 – £55,000 pa

Owns product quality issues in a fast-paced manufacturing setting, leading root cause investigations and corrective actions using 8D, 5 Whys, Fishbone, FMEA and SPC. Partners with Engineering, Production and Supply Chain on continuous improvement, defect prevention, new product introduction and engineering change reviews, in a regulated ISO 13485/9001 environment.

Talentmark · Airdrie · £23 – £26 ph

Lead product definition for technically complex point-of-care systems, managing and coaching a team of systems and requirements engineers. Drive requirements engineering, elicitation and evaluations, and support rapid resolution of technical issues. Fully site-based in Motherwell on a 12-month contract in the medical devices sector.