Regulatory Affairs Specialist II

Regulatory Affairs Specialist II supports the company’s regulatory initiatives to meet strategic short- and long-term objectives. This includes assisting with the preparation and submission of regulatory documents, maintaining compliance with applicable regulations, and supporting cross-functional teams during product development and post-market activities.

Requirements

• Bachelor’s degree in Scientific, Engineering, Public Health, or a related field
• RAPs Certification preferred
• Minimum of 3 years of direct experience in Regulatory Affairs or a related field
• Background in medical devices, biologics, or pharmaceutical industries, medical devices preferred