Roles & Responsibilities
• Handle OOS, OOT, deviations, CAPA, and laboratory investigations
• Review analytical data generated from HPLC, GC, UV, and IR instruments
• Ensure compliance with Quality Management Systems (QMS) and SOPs
• Perform documentation review and maintain data integrity in lab operations
• Use Chromeleon Software 7.2 for chromatography data handling and review
• Support internal, regulatory, and customer audits (FDA, USFDA, MHRA)
• Ensure timely closure of lab incidents and implementation of corrective actions
• Contribute to continuous improvement in laboratory quality systems
Qualification
• B.Pharm / M.Pharm / M.Sc (Chemistry or Analytical preferred)
Experience
• Relevant experience in Pharmaceutical Lab QA / QC environment
Skills
• OOS, OOT, CAPA, deviations handling
• QMS and SOP compliance
• HPLC, GC, UV, IR instrumentation
• Chromeleon Software 7.2
• Regulatory audit exposure (FDA, USFDA, MHRA)
• Documentation and data integrity
About the Organisation
IPCA Laboratories is one of India’s leading pharmaceutical companies with a strong global presence. The company is known for its commitment to quality, regulatory compliance, and excellence in manufacturing, offering professionals a stable and growth-oriented work environment.
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