Document Control
Employbridge · Chatsworth, California, United States · 4 days ago
On-siteAdministrativeFull-time
Specific Responsibilities & Duties
- Promotes a safe working environment and adheres to Health, Safety and Environmental procedures, company safety rules, Current Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) at all times.
- Verifies that each record is accurate and complete, in compliance with GMP practices.
- Assembles Production Records by batch.
- Ensures documentation is reviewed and meets all required testing prior of releasing product in QAD.
- Prepares Documentation for (B, M, E) samples prior to sending to customer for review and approval.
- Prepares and reviews Certificate of Analysis.
- Reviews OTC production reconciliation.
- Prepares and reviews Certificate of Manufacture.
- Prepares labels for customer samples.
- Tracks and reports FG OTC annual product review.
- Replies/follows up with emails and/or customer requests.
- Maintains QC status for more than 5 days and provides feedback on status.
- Reviews documentation and releases to ensure completeness and proper GDP documentation.
- Gathers and collects information as needed from other departments.
- Performs additional duties as instructed by QA Assurance Supervisor.