Regulatory Affairs Specialist

From the original posting

India Accountabilities Support regional regulatory affairs activities by coordinating domestic and international product filings, registrations, and regulatory submissions. Prepare, compile, and maintain technical documentation and regulatory files required for medical device approvals. Coordinate tender-related submissions and prepare responses to audit findings and regulatory inquiries. Monitor changes in Indian regulations and communicate relevant updates to global regulatory teams, including assessments of their potential impact on products and business operations. Collaborate with…