A company is looking for a Regulatory Affairs Associate I.
Key Responsibilities
Manage activities for marketed product variations, including authoring and compiling CMC sections for submission documents
Coordinate activities with functional departments to support regulatory filings
Ensure accuracy and timeliness of CMC dossiers and responses while managing assigned projects
Required Qualifications
Experience in regulatory affairs, specifically with CMC sections
Ability to work in a hybrid role, with onsite presence required on specific days
Familiarity with CTD content and structural requirements for regulatory submissions
Experience with PMA supplements is a plus
Willingness to relocate at own expense if not local
Regulatory Associate • Whittier, California, United States