4 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.
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.
Randstad Construction & Property London
Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.
