109 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 Swansea
Field-based sales role covering South Wales, Cheltenham, Gloucester and Worcestershire, owning key hospital and community accounts for Sports Medicine products. You build strategic account plans, run quarterly business reviews, develop tailored proposals and use CRM data to grow revenue and market share with NHS stakeholders.
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.
Talentmark Wrexham £22 – £29 ph
Translate business requirements into user stories and acceptance criteria, working with a scrum master on story sizing and risk analysis. Participate in release and sprint planning, backlog grooming and sprint reviews, collaborating with software engineers, QA and dev-ops. Focused on clinical trial software such as EDC or eCOA within a 21 CFR Part 11 regulated environment.
Wallace Hind Selection Montpellier, France £45,000 – £48,000 pa
Field-based role owning an established South West England and Wales territory for an international medical equipment manufacturer, selling into NHS and private hospitals across departments such as A&E, Renal, Oncology and Day Surgery. Involves rebuilding a neglected region, developing existing accounts and new business through complex multi-stakeholder procurement processes, with regular travel and trips to France for training and meetings.
Wallace Hind Selection Cardiff £45,000 – £48,000 pa
Field-based role selling a broad portfolio of medical equipment into NHS and private hospitals across South West England and Wales, covering departments such as A&E, Renal, Oncology and Day Surgery. You inherit an established customer base and live opportunities, with autonomy to build new business through complex multi-stakeholder procurement processes, reporting to the UK Managing Director.
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.
Medtronic London £76,800 – £115,200 pa
Designs and builds automated test frameworks for embedded and connected hardware used in operating rooms, covering device software, firmware integrations and hardware-software interaction rather than web or mobile apps. Works with Android AOSP, Linux edge devices and IoT gateways, validating drivers, connectivity, OTA updates and service APIs, and embedding quality gates into CI/CD pipelines alongside hardware, firmware and systems engineers.
Medtronic London £76,800 – £115,200 pa
Designs, builds and maintains a Python-based SaaS platform for project, data and annotation management used by internal machine learning engineers and data scientists. Works with data and platform engineers to handle growing data volumes, and collaborates with stakeholders to define requirements and validate features in an iterative, quality-driven environment.
GE HealthCare United Kingdom, YY9 9YY
Owns GE HealthCare's strategic relationships with NHS Trusts and private clinics across the North East, driving the full sales cycle for medical imaging capital equipment including CT, MR, MI, X-ray and Women's Health. Works within a matrixed organisation alongside a team of Imaging Account Managers, managing CRM forecasting, tender processes and long-term account strategy.
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.
