92 jobs
Johnson & Johnson MedTech Beerse, Belgium €79,800 – €137,770 pa
Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data.
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.
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 London
Field-based sales role covering the London territory, promoting a medical technology product portfolio to NHS and private customers. Involves building customer relationships, identifying growth opportunities, following up leads, and providing technical advice and product training. Suits a new graduate or someone with clinical skills moving into a commercial career.
Medtronic Milan, Italy €31,200 – €46,800 pa
Acts as the primary point of contact for customers throughout 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.
Wallace Hind Selection Watford £35,000 – £40,000 pa
Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region, with 80% new business generation and 20% account development. Involves theatre-based demonstrations, quotations, and attending congresses, with full training and mentoring provided.
Wallace Hind Selection Birmingham £45,000 – £48,000 pa
Field-based new business role selling medical equipment such as stretchers, treatment chairs and examination couches into NHS and private hospitals across the West Midlands and North Wales. You build the territory from the ground up, running product demonstrations and negotiating complex multi-stakeholder procurement processes with clinical, EBME and estates teams.
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.
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.
Vero Hr Cambridge £45,000 – £55,000 pa
As a Quality & Regulatory Specialist, you will support clients in developing medical devices with a strong software focus, ensuring they meet regulatory requirements and quality standards. Your role involves creating and reviewing technical documentation, educating clients on regulatory needs, and collaborating with software engineers and senior stakeholders to deliver practical solutions.
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.
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.
TRS Consulting Reading £45,000 – £55,000 pa
Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets. Home-based with a company car.
TRS Consulting Milton Keynes £45,000 – £55,000 pa
Home-based account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. Involves managing key customer accounts, identifying new business, attending exhibitions and local events, analysing competitor activity and producing proposals and sales agreements to exceed area sales targets.
Matchtech Fareham
Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.
