Job Description

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.)

Job Tags

Full time

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