25 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.
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.
CV Technical Christchurch, New Zealand £60,000 – £65,000 pa
Lead automation projects from concept and specification through commissioning, validation and production release, acting as site subject matter expert for automated assembly equipment. Work with Operations, Quality, R&D and external machine builders on robotics, machine vision, laser marking, leak testing and serialization, while mentoring junior engineers and driving continuous improvement.
Johnson & Johnson MedTech Blackpool
Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.
Johnson & Johnson MedTech Blackpool
Performs physical, analytical and chemical QC testing on raw materials, in-process and finished products, and leads laboratory and non-conformance investigations. The role covers GMP documentation, equipment calibration, method validation and consumable management while ensuring compliance with ISO 13485, ISO 14001 and FDA QMSRs. It also involves training other staff and liaising with approved manufacturers to keep testing on schedule.
Medtronic London £76,800 – £115,200 pa
Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.
OrganOx Oxford
Leads a team of Windows software engineers building device-hosted applications and services for Class II and III medical devices, covering GUI development, connectivity and cybersecurity mitigations. Owns the full SDLC, regulatory compliance (FDA, ISO 13485, IEC 62304), roadmaps, budgets and hiring, while acting as technical representative to regulators, partners and customers.
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.
Ripple Luton £65,000 pa
Hands-on operational leadership across manufacturing, quality assurance, supply chain, purchasing and facilities at a medical equipment manufacturer. Sits on the Senior Leadership Team, owning site health and safety, ISO compliance and continuous improvement, while partnering with executive leadership on business planning and representing the site at group forums.
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 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.
