• Review and approval of batch manufacturing records and batch packing records
• Ensure compliance with cGMP, SOPs, and regulatory requirements
• Handle deviations, change controls, CAPA, and OOS/OOT investigations
• Support internal, external, and regulatory audits
• Review validation, qualification, and stability documents
• Ensure data integrity and documentation accuracy for injectable products
• Coordinate with Production, QC, and Engineering teams
• Graduate in Pharmacy
• 4 – 8 years in DQA (Injectables)
• Documentation review (BMR/BPR)
• Deviation, CAPA & change control handling
• cGMP & regulatory compliance
• Injectable QA operations
• Audit handling & data integrity
Aspiro Pharma is a USFDA-approved pharmaceutical company specializing in injectable formulations. The company focuses on quality-driven manufacturing and offers growth opportunities in regulated environments.
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