QA Associate( OSD Pharma Experience required)
About the role
Review and release of batch records, shipper labels, expiry forms, lot memos, and proofs. Approve new MBRs and change controls. Track batch record releases and release finished products, labels, and cartons in SAP. Manage incoming labels and cartons, including sampling, inspection, and release. Conduct Kenvue batch reviews, upload documents to the SAP Portal, and log weekly Kenvue batch releases. Prepare annual product reviews and submit annual report data to the GIL Team for FDA submission. Create stability initiation forms, coordinate sample collection and shipping to customers, and manage customer queries. Share change controls with customers and follow up. Log change controls and provide role-based training for new employees. Support audits by reviewing documents for accuracy and compliance.
Requirements
- Experience in a GMP environment is preferred
- Strong communication skills
- Attention to detail
- Proficiency in Microsoft Excel
Pay
$50,000 - $60,000 per year