The Regulatory Affairs Specialist will plan and execute global regulatory activities necessary to obtain and maintain regulatory approvals in the US and International markets. In this role, you will ensure compliance with relevant regulations, guidance, and standards, including EU Medical Device Regulation, ISO and other US and global regulations for dental and orthodontic products. You will support the RA team to interact with regulatory authorities to assure timely new product introductions, registration and licensing and continued product access globally. The Regulatory Affairs Specialist will assist in providing regulatory review of labeling and advertising, design changes, and specification changes as well as prepare technical documentation that complies with all applicable regulations.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
1-10 employees