Product Regulatory Affairs Intern

- Responsible for quality compliance in accordance to medical regulatory standards.
- Work closely with other internal departments to assure and validate the project process.
- Responsible for obtaining and maintaining quality standards and regulatory certifications.
- Work directly with engineering team to understand project concept, objectives, and approach.
- Gain deep understanding of problem statements from medical professionals and users, identify needs and product gaps.
- Ensure development team complies with technical documentation in accordance to medical certification standard and company`s regulatory strategy.

- Must be organized and detail-oriented.