Medical Technology Jobs

Johnson & Johnson MedTech · Spring House, United States · US$137,000 – US$235,750 pa

Leads the Accelerando program management function, acting as a trusted advisor to Compound Development Teams to de-risk and accelerate priority drug development programs. Facilitates cross-functional project planning in Planisware, conducts critical path and threat/opportunity analyses, and drives best practices and process improvements across a global matrix organisation.

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads the Accelerando program management function, partnering with high-priority new product development teams to de-risk and accelerate clinical trial execution. Acts as a trusted advisor to Compound Development Teams, running critical path analysis, threat and opportunity assessments, and project planning in Planisware and MS Project. Also leads a team, drives best-practice adoption and benchmarking across a global matrix organisation.

Smith & Nephew · Watford

Leads the design and delivery of AI-enabled supply chain planning solutions on Kinaxis Maestro, owning architecture for advanced forecasting, intelligent planning workbooks and autonomous agents. Partners with business and IT stakeholders, runs workshops and mentors colleagues while defining data integration and governance standards.

Smith & Nephew · Derby

Field-based clinical sales role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Involves hands-on clinical support, education and relationship building with community healthcare professionals, guiding decision makers and strengthening advocacy for therapies across the territory.

Medtronic · London · £76,800 – £115,200 pa

Builds and maintains modern C++ (C++17+) application software for intra-operative surgical devices, working in a multidisciplinary team spanning embedded, cloud and application software. Responsibilities include device monitoring, cloud connectivity, debugging, and developing secure, medical-grade code compliant with regulatory and security processes.

Spectrum IT Recruitment · Southampton · £50,000 – £60,000 pa

Hands-on role combining project delivery, commercial and financial oversight, people management and quality/regulatory compliance within a small medical-sector business. You will lead business projects, manage resources and risks, support strategic planning, monitor budgets and expenditure, and maintain compliance with medical device regulations while building customer, supplier and partner relationships.

VK Recruitment · Belfast · £50,000 – £65,000 pa

Oversee complex production workflows in a specialist dental laboratory, providing technical leadership across CAD/CAM, milling, 3D printing, PMMA, zirconia and ceramics. Troubleshoot equipment and software issues, improve efficiency and quality, and coach technicians and departmental leads. Reports to the Associate Director after a structured induction.

Intersurgical · Wokingham · £29,000 – £32,000 pa

Manufacturing role producing medical devices to work instructions and weekly targets while following quality and health & safety procedures. Involves heavy and prolonged lifting plus dexterous tasks needing good hand-eye coordination, working at a fast pace to meet deadlines. Full training provided; based in the Manufacturing Department on continuous rolling shifts.

HAYS Specialist Recruitment · Oxford

Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.

Planet Recruitment · Abingdon · £28,000 – £35,000 pa

Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.

SGS · United Kingdom · £30,000 – £32,000 pa

Coordinate and support technical documentation reviews for the UK Medical Devices team, managing review processes, monitoring KPI reports and driving resultant actions. Handle complaints, raise purchase orders for client invoicing, and strengthen key client relationships through calls and meetings. Requires practical experience of Medical Device Regulations or auditing regulations and strong documentation control.

Talentmark · Stirling · £25 – £27 ph

Execute complex experimental workstreams from concept through to design transfer, analysing multi-factorial data and presenting technical findings to stakeholders. Apply Design for Manufacture principles to optimise product formulations and characterisation, while upholding GLP, GMP and GDP compliance in a fully site-based laboratory. Requires diagnostic immunoassay expertise, ideally with particle-based assays and fluorescent detection.

Ernest Gordon Recruitment · Andover · £40,000 – £45,000 pa

Maintains and develops the quality management system in a high-end cleanroom, ensuring compliance with ISO 9001, ISO 13485 and AS9100, with training provided where needed. Uses CAPA, 8D and 5 Whys to drive quality standards, supported by a team of six. Works Monday to Thursday 8:30am-5pm with an early Friday finish.

Talentmark · Welwyn Garden City · £38 – £60 ph

Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.

Nomad Mediation · United Kingdom · £40,000 – £45,000 pa

Reporting to the Quality Manager, you will maintain and improve a supplier approval system across ISO 9001, ISO 13485, BS EN 14065, ISO 14001 and ISO 50001. The role involves planning and performing external supplier audits, including international travel, closing out corrective actions, and partnering with Procurement on supplier selection and risk. You will also run internal audits and monitor Supplier Quality KPIs and CAPAs.