Regulatory Affairs Managers, Bayonne NJ


  • Manage and coordinate implementation of all regulatory and quality management systems requirements across all brands reflective of both the FDA CFR section 111 and the Company's policies and practices which includes making sure the Company is fully compliant and meeting all requirements for product registrations (dietary supplements).
  • Management of cGMP Quality systems (i.e., SOP's, SOP Training, Adverse Events Reporting, Document Control).


To apply, please send your resume to:

Summit Rx Inc

56 New Hook Rd

Bayonne, NJ 07002

Or email: