Quality Systems Specialist: Compliance & Improvement
Meridian Bioscience Inc.
Meridian Bioscience Inc. is seeking a Quality System Specialist to support and improve the QMS within a regulated medical device/IVD environment. The role ensures compliance with 21 CFR Part 820, ISO 13485, cGMP, and Good Documentation Practices while leveraging data analysis to drive improvements. The candidate will collaborate with Manufacturing, R&D, Regulatory Affairs, Product Support, and Supply Chain, among others, to maintain inspection readiness and strong quality performance. #J-18808-Ljbffr Meridian Bioscience Inc.
Vacancy posted 1 day ago
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