Regulatory Affairs Specialist

CEDENT

Boston, MA

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JOB DETAILS

SKILLS

Biology, Chemistry, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, FDA (Food and Drug Administration), FDA Requirements, Organizational Skills, Pharmacy, Regulations, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Team Player, United States Drug Enforcement Agency (DEA)

LOCATION

Boston, MA

POSTED

30+ days ago

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.)

Regulatory Affairs Specialist

CEDENT

Boston, MA

About the Company

CEDENT

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