QA Associate - Pharmaceutical Manufacturing
GranulesManassas, Virginia, United States
Posted September 18, 2025
Full Time
About the Company
Granules is a healthcare and manufacturing company that specializes in private label over-the-counter generic pharmaceuticals. It offers quality assurance, compliance, and sales support services to ensure high standards and affordable pricing for its clients.
Job Description
The QA Associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications in a pharmaceutical manufacturing setting. This role involves inspecting, reviewing, and maintaining document control systems, batch records, and quality system functions, while adhering to relevant laws. Knowledge of cGMP and FDA regulations is essential.
Requirements
- Manage and maintain company document control and archival systems (hardcopy and electronic)
- Manage and route, review, approve, distribute and archive controlled documents
- Track controlled documents through document control number issuance, audit file status reports
- Archive and maintain batch records and audit files
- Control labeling components and ensure proper labelling
- Perform and support maintenance of documents like reports and CAPAs
- cGMP Compliance in Document Control
- Problem solving and resolving complex issues