QC - Raw Material - Executive

? 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.