7 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.
Johnson & Johnson MedTech Maidenhead
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.
Johnson & Johnson MedTech Raritan, United States US$137,000 – US$235,750 pa
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.
Technical Placements Gloucester £65,000 pa
Hands-on international sales role focused on recruiting, onboarding and developing distributor and agent partners across Europe and Latin America for a specialist healthcare manufacturer. Reporting to the General Manager, you will research new markets, negotiate agency agreements, set sales targets and manage partner performance through CRM, with regular international travel.
Evolve Selection Hemel Hempstead
Leads the UK Medical Affairs strategy for an aesthetics organisation, developing integrated brand medical plans and feeding medical insight into a three-year business strategy. Drives evidence generation, publication planning, real-world evidence and KOL engagement while building scientific capability across Commercial and Marketing. Manages a multidisciplinary Medical Affairs team and reports to the Country Manager.
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.
Johnson & Johnson MedTech Horsham, United States US$137,000 – US$235,750 pa
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.
Johnson & Johnson MedTech Titusville, United States US$137,000 – US$235,750 pa
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and evaluations. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with oversight of deliverables prepared by other team members.
