Senior Executive-Quality Control

Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. - Perform composite and individual sampling as per standard operating procedures (SOPs). - Conduct physicochemical testing of APIs and excipients based on IP, BP, USP, Ph. Eur., or in-house specifications. - Carry out tests such as identification (FTIR/UV/chemical tests), assay, pH, loss on drying, sulphated ash, heavy metals, etc. - Ensure compliance with material specifications and standard testing procedures (STPs)/SOPs for each product. - Verify vendor Certificates of Analysis (COAs) and investigate any discrepancies. - Record test results in analytical reports/raw data sheets. - Prepare Certificate of Analysis (COA) for approved raw materials. - Maintain proper filling and signing of all logbooks, registers, and worksheets. - Collaborate with Quality Assurance (QA) for material release tagging. Qualifications Required: - B.Sc. / M.Sc. in Chemistry or Pharmaceutical Chemistry. Additional Company Details: (Omit as no additional details are provided in the job description),