QARA (Quality Assurance and Regulatory Affairs) Program Manager (x/f/m)

Doctolib is seeking a QARA (Quality Assurance and Regulatory Affairs) Program Manager to join our team. In this role, you will be instrumental in ensuring our products meet the highest quality standards and comply with all relevant regulatory requirements. As part of our commitment to building the healthcare we all dream of, you will collaborate closely with cross-functional teams to drive quality and compliance initiatives.

Your primary responsibilities will include developing and implementing quality assurance strategies, overseeing regulatory compliance processes, and managing audits and inspections. You will work closely with product development teams to integrate quality and regulatory considerations into the product lifecycle, ensuring that all products meet both internal standards and external regulations.

The ideal candidate will have a strong background in quality assurance and regulatory affairs within the healthcare or medical device industry. You should possess excellent project management skills, a deep understanding of relevant regulations and standards, and the ability to effectively communicate and collaborate with diverse teams.

At Doctolib, we offer a dynamic and inclusive work environment where your contributions directly impact the improvement of healthcare services. We provide opportunities for professional growth and development, along with a comprehensive benefits package designed to support your well-being.