? Raw Material Testing: Perform physicochemical and instrumental analysis (HPLC, GC, UV, FTIR, Titrations) of raw materials and excipients.
? Compliance & Documentation: Maintain test records, COAs, and laboratory documentation as per GMP, GLP, and data integrity guidelines.
? Sampling & Specifications: Ensure proper sampling, handling, and release of raw materials as per approved specifications.
? OOS & Deviation Management: Investigate out-of-specification (OOS) results, deviations, and laboratory incidents, implementing CAPA as required.
? Audit Readiness: Support regulatory audits (USFDA, MHRA, WHO, EU-GMP) by ensuring QC compliance and preparing required documentation.
📌 QC - Raw Material - Executive (India)
🏢 USV
📍 India
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