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.

FIELD · Brecon · £33,000 – £38,000 pa

This role involves hands-on troubleshooting, maintenance, calibration, and repair of medical equipment both onsite and remotely within a leading hospital environment. The engineer will perform preventative maintenance, equipment upgrades, and ensure compliance with manufacturer guidelines and contractual KPIs. The position supports critical healthcare operations by maintaining the reliability and safety of advanced medical devices.

OrganOx · Oxford

Designs mechanical components and assemblies for medical devices using CAD tools, supporting analysis, testing and design verification and validation. Works with manufacturing, suppliers and cross-functional electrical, software and quality teams through the product development lifecycle, preparing documentation to ISO 13485 and participating in risk management and design reviews. Office-based in Oxford with flexibility.

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.

Medtronic · London · £124,800 – £187,200 pa

Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise partnerships and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability, analytics and monitoring platforms. Remote with around 70% regional travel.

Industrious Recruitment · Milton Keynes · £37,500 pa

Provide first-line remote technical support for specialist laboratory analysers and medical devices, diagnosing faults using remote-access tools such as RDP, VNC and augmented reality. Work with laboratory staff, field service engineers and product specialists to resolve issues and minimise on-site visits, while training users and maintaining service records.

GE HealthCare · United Kingdom, YY9 9YY

Defines and executes the Molecular Imaging modality strategy across the UKI zone, owning positioning, pricing and profitability for PET-CT, Nuclear Medicine and Radiopharmacy. Leads a team of Modality Sales specialists, coordinates forecasting and tender responses, and acts as the interface between local markets and the International MI marketing team.

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.

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.