Regulatory Affairs Project Lead – NDA Submissions & MDR

Anika Therapeutics, Bedford, MA, is seeking an Regulatory Affairs Project Manager/Sr. Manager to lead cross-functional regulatory programs for pharma, biotech and medical device products.

You will plan, execute, and coordinate NDA submissions, CMC activities, and regulatory strategies across global teams. The role requires strong project management, NDA and CMC knowledge, and the ability to influence without direct authority.