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Your mission
Your Mission: You will take ownership in the development of regulatory strategies, submissions, and regulatory documentation to ensure compliance with global standards. Key tasks include:
- Develop and execute regulatory strategies aligned with business objectives
- Create, submit, and maintain regulatory documentation, including technical files and submissions required for compliance, in liaison with Research & Development
- Liaise with notified bodies, health authorities, and other relevant stake holders on behalf of the organization
- Monitor and interpret regulatory changes and ensure products adhere to evolving requirements
- Integrate regulatory requirements into product development through cross-functional collaboration
- Conduct literature reviews and clinical evaluations
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