QA Associate( OSD Pharma Experience required)

Granules • Manassas, VA

10d

About The Position

The QA Associate will be responsible for a variety of tasks related to batch record review and release, label and carton approval, and ensuring compliance with GMP standards. This role involves working with SAP, preparing reports, and supporting audits.

Requirements

• OSD Pharma Experience required
• Experience in GMP environment is preferred
• Communication skills and attention to detail
• Microsoft Excel

Responsibilities

• Batch Record Review and Release
• Shipper Labels Review and Approval
• Expiry Form Creation and Approval
• Lot Memo Review and Approval
• Print Proofs Review and Approval
• New MBR’s and Change Control Approvals
• Keep track of Batch Record releases
• Release Finished products, Labels, and Cartons in SAP
• Incoming Labels and Cartons Sampling, Inspection and Release
• Kenvue Batch Review and Release and upload the documents in SAP Portal
• Logging and Reporting Weekly Kenvue Batch Releases
• Preparing Annual Product Review for the products
• Prepare and submit Annual Report Data to GIL Team for FDA Submission
• Stability Initiation Forms Creation
• Sample Collection and Shipping to Customers
• Customer Query Management
• Sharing Change Controls with the Customers and follow-up
• Logging Change Control
• Providing role-based new Employee Training
• Supporting audits by reviewing documents for accuracy and compliance

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed