6 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.
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.
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 Zuchwil, Switzerland
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 governing 3PL and vendor technology obligations. Leads a cross-country team and influences senior stakeholders in a complex global matrix.
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.
Planet Recruitment Abingdon £28,000 – £35,000 pa
Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.
