92 jobs
Bluetree Cambridge £65,000 – £80,000 pa
Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.
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.
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.
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.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing biomedical and aesthetic laser equipment across a London patch, with occasional UK travel and roughly two nights away per month. The engineer receives manufacturer-funded training and certification on high-complexity medical lasers, with a progression plan toward senior positions. Working Monday to Friday, 40 hours per week, with time off in lieu for excess hours.
Adecco Welwyn Garden City £377 – £500 ph
Coordinate early-phase clinical trials within a pharmaceutical Clinical Operations team, covering study start-up, feasibility, timelines, recruitment and vendor oversight. Maintain TMF documentation, risk logs and regulatory compliance under ICH-GCP while working with Data Management, Regulatory Affairs and external partners.
Adecco Surrey £200 – £300 pd
Supports a global pharmaceutical organisation's digital health strategy by identifying and evaluating early-stage opportunities that combine digital technology with healthcare products. Day to day involves market research, business case and value proposition development, external partner assessment, and Agile activities such as sprint planning and OKR reviews, working with commercial, medical, technology and brand teams.
Philips United Kingdom - Remote Based £53,410 – £83,930 pa
Leads customer-facing Radiology Informatics programs covering PACS, RIS and enterprise imaging, managing software implementations from order signature through go-live and handover. Runs large cross-functional projects with budgets typically over £1M, handling scope, risk, budget and stakeholder governance. Field-based across the UK, Ireland and Nordics, working from home with around 60% travel to customer sites.
Clearline Recruitment Ltd Welwyn Garden City £377 – £550 pd
Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.
Impact Recruitment Aldershot £45,000 – £55,000 pa
Hands-on mechanical design role taking safety-critical respiratory protective equipment from concept through 3D CAD modelling, prototyping, testing and production. Involves detailed drawings, DFMEA, jig and fixture design, NPI and technical support, working closely with manufacturing, quality, customers, suppliers and external test organisations.
GE HealthCare Hatfield
Lead a team of technicians in a repair centre, coordinating daily workloads while hands-on repairing and troubleshooting Patient Care Solutions and Ultrasound systems down to component level. Prepare quotations, manage parts and inventory, install and test hardware and software, and ensure ISO 9001 compliance and customer communication.
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.
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.
SRG Lancashire
Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.
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 Titusville, 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, and serves as the primary contact for YODA Project requests, supporting external research teams using clinical study data.
