QA Associate( OSD Pharma Experience required)

Description

• 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

Requirements

• Experience in GMP environment is preferred
• Communication skills and attention to detail.
• Microsoft Excel