Medical Technology Jobs

Johnson & Johnson MedTech · High Wycombe

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedural requirements. Supervises vendors handling data anonymization and synthetization, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data and leads cross-functional projects within a matrix organization.

Johnson & Johnson MedTech · Wokingham

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Directs a Business Adoption team covering change impacts, communications, training, readiness, role mapping and sustainment, advising programme and business leaders on adoption risks and pace of change.

Smith & Nephew · UK - Field

Field-based sales role covering South Wales, Cheltenham, Gloucester and Worcestershire, owning strategic accounts and driving revenue growth for Sports Medicine focus brands. Involves quarterly business reviews, tailored proposals, CRM data analysis and engagement with senior clinical and NHS procurement stakeholders.

Smith & Nephew · Stoke-on-Trent

Field-based clinical specialist role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Combines hands-on clinical support, education of community healthcare professionals, relationship building and territory management to drive adoption of therapies such as NPWT.

Medtronic · London · £95,200 – £142,800 pa

Builds and maintains the internal platform tooling that other engineering teams rely on, spanning Infrastructure as Code with OpenTofu, EKS and Helm, CI/CD automation, and observability with OpenTelemetry. Also supports AI agentic workflows and designs pragmatic fixes for developer productivity gaps, mentoring engineers across the organisation.

Platform Recruitment · Cambridge · £35,000 – £45,000 pa

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA functionality and C for low-level hardware control, integrating and debugging digital electronics across the full product lifecycle alongside hardware and software engineers.

QIAGEN · Manchester

Lead the global Medical Affairs strategy for an oncology precision diagnostics portfolio, shaping biomarker and companion diagnostic initiatives with pharma and biotech partners across the drug development lifecycle. Engage key opinion leaders and cross-functional teams in a matrixed international environment, representing the company at conferences and advisory boards.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

OrganOx · Oxford

Designs and develops electronic circuits and PCB layouts for medical devices, taking full lifecycle ownership from concept through to manufacturing handover. Work covers schematic capture, component selection, prototyping, debugging and verification against IEC 60601, collaborating closely with mechanical, software and systems engineers. Based on-site in Oxford with some remote design work.

SoCode · Cambridge · £400 – £500 pd

Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.

Morgan McKinley · Bampton · CA$40,000 – CA$50,000 pa

Hands-on role bridging R&D and production for next-generation fluidic products, building, wiring and commissioning assembly fixtures, automated test equipment and robotic cells. Involves process scale-up (precision dispensing, laser welding, leak testing), equipment validation (FAT/SAT, IQ/OQ/PQ) and continuous improvement using root-cause analysis and SPC. Works alongside senior engineers in a fully on-site manufacturing environment.

Reed · Southampton · £28,000 – £35,000 pa

Hands-on warehouse role combining physical duties with stock control and systems work for a medical device manufacturer. You will manage inventory accuracy, goods receipt, picking and dispatch, and help develop SAP and WMS processes alongside the Operations Director. Distinct for its blend of floor work and administrative process improvement.

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.

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.