job summary: As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with FDA and global regulatory requirements while supporting the efficient and cost-effective manufacturing of high-quality medical devices. This role involves managing regulatory documentation, coordinating global submissions, and assisting internal teams to meet corporate registration objectives. Your expertise will help drive timely approvals and ensure ali
job summary: As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with FDA and global regulatory requirements while supporting the efficient and cost-effective manufacturing of high-quality medical devices. This role involves managing regulatory documentation, coordinating global submissions, and assisting internal teams to meet corporate registration objectives. Your expertise will help drive timely approvals and ensure ali
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