We are seeking a detail-oriented and proactive Regulatory Affairs Specialist to support regulatory compliance activities for In Vitro Diagnostic (IVD) products. The role is responsible for managing and verifying Product Information Management (PIM) data, supporting regulatory submissions, and ensuring the accuracy and consistency of product information across internal systems and regulatory documentation.
The successful candidate will collaborate with cross-functional teams including Regulatory Affairs, Labeling, Quality, Supply Chain, and Marketing to maintain high-quality product data and support global regulatory requirements
Source: HCLTech careers — Read the original posting and apply
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