Senior QARA Specialist – MedTech Compliance

PQE Group is seeking an experienced Quality Assurance & Regulatory Affairs professional to support a Medical Device organization. You will act as an extension of the manufacturer's quality and regulatory team, ensuring compliance with EU MDR 2017/745 and ISO 13485/9001/14001. The role involves hands-on quality and regulatory activities across audits, CAPAs, deviations, and post-market surveillance, with opportunities to collaborate on international projects and product registrations. #J-18808-Ljbffr