Sr Regulatory Executive

• Develop and implement regulatory strategies to ensure compliance with EU MDR 2017/745.
• Prepare and review regulatory submissions, including technical documentation and clinical trial applications.
• Collaborate with cross-functional teams to ensure timely and successful product approvals.
• Conduct thorough reviews of regulatory documents to identify areas for improvement.
• Provide guidance and support to internal stakeholders on regulatory matters related to EU MDR 2017/745.
• Stay up-to-date with changes in regulatory requirements and industry trends.

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