Anika Therapeutics, Inc. seeks a Regulatory Affairs Project Manager/Sr. Manager to lead cross-functional regulatory programs for pharma, biotech, and medical device products.
You will own regulatory planning, execution, submission readiness, and program coordination across global teams. The role requires NDA experience, CMC knowledge, and strong project-management skills to meet timelines while aligning with global regulatory strategies and business goals.
#J-18808-LjbffrSenior Regulatory Programs Manager - NDA Submissions in bedford at Unknown Company
This position is listed as full time and onsite.