Seeking a Regulatory Affairs Expert to drive product approvals and ensure compliance with regulations.
About the Role
* Foster strong relationships with cross-functional teams to facilitate product launches and regulatory submissions.
Requirements:
* A minimum of 5 years' experience in a similar role within the medical device industry;
* Demonstrated expertise in managing global regulatory submissions, including CE marking, FDA clearance, and post-market surveillance;
* Possess excellent communication skills to articulate complex technical information effectively.
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