Part Time
$8/hr
TBD
Aug 31, 2026
We are seeking a knowledgeable and organized Regulatory Affairs Specialist to ensure company products comply with applicable regulatory requirements and quality standards. This role is responsible for preparing regulatory submissions, maintaining compliance documentation, and supporting interactions with regulatory agencies. The ideal candidate will have a strong understanding of FDA 21 CFR Part 820, ISO 13485, and medical device regulatory requirements, along with the ability to collaborate effectively across Quality, Engineering, Manufacturing, and Operations teams. A Bachelor's degree in Engineering or a related technical discipline is required.