Description

Our client, a leading group in the field of medical devices, is looking for a Global Senior QA Manager to join their site based in the canton of... Responsibilities at the site management, you are the guarantor of the compliance with the X system requirements. You will be responsible for: Acting as the Quality Management / PRRC of the site, leading Quality and providing clear direction to the QA team, ensuring excellence across all quality processes: NC / CAPA, Change Control, Risk Management, Complaint Handling, closely collaborating with site leadership and product managers to deploy concrete quality plans, developing a quality culture and GMP X across the site, managing and coordinating all internal & external audits (authorities, notified bodies, clients), actively leading or contributing to quality projects and processes, networking with other group Quality managers to drive evolution. Requirements: Bachelor's or master's degree in biology, pharmaceutical sciences, or equivalent discipline. Confirmed expertise in QMS X medical IVD and standards: ISO, QMSR / 21 CFR 820, MDSAP, IVDD / IVDR. Minimum of 10 years of experience in Quality Assurance in a medtech / healthcare environment, including direct experience in IVD. At least 8 years of successful managerial experience in team development. Recognized leadership, excellent skills, and ability to structure, prioritize, and deliver in a demanding environment. Strong experience in audits and regulatory inspections. Experience in Lean / Six Sigma, X Belt = experience in quality project management. Fluent in French, excellent in English, German appreciated. jid73b3753aen jit0206aen jpiy26aen