Quality & Regulatory Associate

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality & Regulatory Associate based in United States.

This part-time, entry-level role supports the quality and regulatory functions behind innovative products designed to improve women’s health and well-being.
You’ll gain hands-on experience across complaint investigations, material compliance, regulatory documentation, and quality system activities.
The role combines analytical work, technical documentation, and collaboration with engineering, supply chain, and other cross-functional teams.
You’ll help investigate product issues, identify root causes, and maintain accurate records that support product safety and reliability.
You’ll also contribute to international regulatory activities and ensure technical documentation remains complete, accurate, and audit-ready.
This is an opportunity to build practical experience in medical devices, quality engineering, and regulatory compliance within a fast-paced environment.
The position offers flexible remote work in the US, with a part-time schedule of 15–20 hours per week.