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.)
