Regulatory Affairs Specialist (Boston, MA)

CEDENT
Boston, MA
Role Description
This is a full-time on-site role for a Regulatory Affairs Specialist located in Torrance, CA. The Regulatory Affairs Specialist will be responsible for regulatory documentation, compliance, requirements, submissions, and overall regulatory affairs activities.
Qualifications
  • Regulatory Documentation and Regulatory Compliance skills
  • Understanding of Regulatory Requirements and Regulatory Affairs
  • Strong attention to detail and organizational skills
  • Ability to work effectively in a team environment
  • Knowledge of FDA regulations and guidelines
  • Knowledge of cGMP
  • Comfortable working directly for regulatory agencies, including the Food and Drug Administration (FDA), DEA, and Boards of Pharmacies
  • Bachelor's degree in a relevant field (pharmacy, biology, chemistry, etc.)

Posted 2025-08-19

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