Sr. Regulatory Executive

• Develop and implement regulatory strategies to ensure compliance with EU MDR 2017/745 regulations.
• Conduct thorough analysis of regulatory requirements and provide guidance on compliance matters.
• Collaborate with cross-functional teams to ensure timely submission of regulatory documents.
• Prepare and review regulatory submissions, including technical documentation and clinical trial applications.
• Ensure ongoing monitoring and reporting of regulatory activities.
• Provide training and support to internal stakeholders on regulatory affairs matters.

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