Director, Regulatory Affairs

Clova Health specializes App based SaaS wellness coaching for metabolic health including obesity and pre-diabetes population with the support of advanced continuous glucose monitoring products.  It offers the advantage of real-time data-driving artificial intelligence for advice on diet, exercise, and other factors.

Responsibilities

  • Develop and manage regulatory strategy for OTC medical device products
  • Manage the regulatory affairs operations
  • Draft and review regulatory documents as necessary
  • Interact with various government agencies
  • Ensure compliance with all applicable   regulations

Qualifications

  • Advanced training in life sciences or related field
  • Minimum 7 plus years of experience in OTC medical device industry and a minimum of 3 years in management positions
  • Proven track record in the launch of new OTC medical devices
  • Extensive knowledge and experience in regulatory interactions with government agencies
  • Excellent communication and personal skills

Part-time, flexible schedule, and competitive benefits.

To apply, send your CV to support@clovahealth.com