CEDENT- Regulatory Affairs Specialist (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.)

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