Quality Control Executive

Role & responsibilities

• Conduct chemical and physical analysis of raw materials, intermediates, and finished products using analytical instruments (HPLC, GC, UV, FTIR, Dissolution, etc.).
  
• Prepare and review analytical reports, Certificates of Analysis (CoAs), and maintain accurate laboratory records.
  
• Perform routine and non-routine analysis in compliance with pharmacopeias (USP, BP, IP, EP) and internal specifications.
  
• Ensure timely calibration, maintenance, and qualification of laboratory instruments.
  
• Conduct stability studies and support product shelf-life monitoring.
  
• Participate in investigations of OOS (Out-of-Specification), OOT (Out-of-Trend), and deviations, and assist in implementing CAPAs.
  
• Maintain compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  
• Support regulatory inspections and audits (USFDA, MHRA, WHO-GMP, etc.).
  
• Coordinate with QA, Production, and R&D teams for quality-related issues.

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