Regulatory Affairs Associate

Entry Level
Main Office
Posted 6 days ago
Job Summary

The Document Control Specialist is responsible for managing, reviewing, and maintaining controlled documents related to pharmaceutical operations. The role requires a licensed pharmacist with hands-on experience in FDA applications, regulatory submissions, and document compliance to ensure all records meet regulatory and quality standards.
Key Responsibilities:

• Manage and control all regulated documents in compliance with FDA and internal quality standards
• Review, organize, and maintain regulatory documents related to FDA applications, licenses, and renewals
• Ensure accuracy, completeness, and consistency of controlled documents prior to submission
• Coordinate with regulatory, quality assurance, and operations teams for document updates and approvals
• Track document versions, revisions, and archival in accordance with document control procedures
• Support audits, inspections, and regulatory inquiries by providing required documentation
• Monitor regulatory changes and ensure documentation aligns with updated FDA guidelines
• Ensure timely submission and proper filing of regulatory and compliance-related documents
Qualifications / Requirements:

• Bachelor’s Degree in Pharmacy
• At least 1–3 years of experience in document control, regulatory affairs, or quality compliance
• Hands-on experience with FDA applications, submissions, or renewals
• Strong knowledge of FDA regulations and pharmaceutical documentation standards
• Detail-oriented with strong organizational and document review skills
• Proficient in MS Office and document management systems

Job Features

Job CategoryGregan 101 Medical
Benefits:- HMO with Dental Benefit - Free Parking - Paid Leave

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