Responsible for regulatory compliance of Meridian’s product realization process for the company’s growing line of in vitro diagnostic (IVD) products; this position will also support ongoing product conformity requirements. Ensure products are designed and manufactured in a manner consistent with risk management strategies and regulatory requirements throughout all stages of the product lifecycle (research, development, transfer, validation/verification, labelling, regulatory application and maintenance). Works cross-functionally to ensure risk and compliance standards are clearly defined Responsibilities May Include: Ensures that national and international medical device and ISO compliance regulations for the design and development of medical devices
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