NanoFCM CO., LTD Stevenage £26,000 – £40,000 pa
Field-based role installing, maintaining and servicing nano-flow cytometry instruments at customer sites across the UK and Europe, plus remote phone and email troubleshooting of hardware, software and reagents. Involves preventative maintenance scheduling, service documentation, spare parts inventory and coordinating service contracts with the sales team, following training with senior technical staff.
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 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.
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 High Wycombe
Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.
