13 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 Beerse, Belgium
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners to ensure successful release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, and operational readiness including SOPs and user access management. Serves as the business process single point of contact for PLAN stakeholders through hypercare and post-go-live stabilization.
Johnson & Johnson MedTech Madrid, Spain
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners on release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, operational readiness, and hypercare for a multi-year SAP S/4HANA supply chain transformation.
OrganOx Oxford
Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.
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.
Newton Colmore Cambridge
Design and develop complex medical devices as part of a multidisciplinary team of mechanical engineers, physicists and electronics engineers. The role is hands-on, spanning CAD, prototyping and functional mechanism design across multiple medical specialisms, including some surgical robotics, with variety rather than a single-device focus.
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.
Medtronic Edinburgh £76,800 – £115,200 pa
Own the end-to-end data lifecycle for an AI and algorithm R&D team, from clinical study data collection through validation trials. Design and manage scalable infrastructure across clinical trials, sensor platforms and HPC environments, building ETL/ELT pipelines and data tooling in Python and SQL while shaping data architecture standards.
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.
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.
SGS United Kingdom £30,000 – £32,000 pa
Coordinate and support technical documentation reviews for the UK Medical Devices team, managing review processes, monitoring KPI reports and driving resultant actions. Handle complaints, raise purchase orders for client invoicing, and strengthen key client relationships through calls and meetings. Requires practical experience of Medical Device Regulations or auditing regulations and strong documentation control.
Talentmark Stirling £25 – £27 ph
Execute complex experimental workstreams from concept through to design transfer, analysing multi-factorial data and presenting technical findings to stakeholders. Apply Design for Manufacture principles to optimise product formulations and characterisation, while upholding GLP, GMP and GDP compliance in a fully site-based laboratory. Requires diagnostic immunoassay expertise, ideally with particle-based assays and fluorescent detection.
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.
