4 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.
SRG Lancashire
Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.
Yolk Recruitment Bridgwater £55,000 pa
Owns quality operations across a precision manufacturing site, maintaining QMS, certifications and audit readiness while leading continuous improvement. Acts as main contact for customers, auditors and suppliers, managing non-conformances, root cause investigations and corrective actions using SPC, PFMEA, PPAP and 8D. Also supports day-to-day Health & Safety activities alongside Production and Engineering teams.
Platform Recruitment London
Develops and optimises therapeutic delivery formulations, running lab-based in vitro studies and analytical characterisation to assess stability and performance. Works in a multidisciplinary team progressing early-stage technologies toward manufacturing, with external partner collaboration and scale-up considerations.
