CQA Executive

What You Become a Part Of

Join our Quality team to support QMS activities, quality compliance, change controls, deviations, rejection management, and quality review processes at the Pawane manufacturing site.

What To Expect

• Manage Change Controls including review, evaluation, execution, post-implementation checks, and closure tracking.
• Handle Deviations from review and evaluation through completion of recommended actions and closure.
• Manage material rejection activities , including SAP destruction notes, approval, and tracking until physical destruction.
• Prepare Inspection Plans for Semi-Finished Goods in SAP as required.
• Prepare and calculate Pawane Quality Index for QMS-related parameters on a monthly basis.
• Compile quality data for Monthly Quality Review Meetings, Monthly Presentations, and Quality Council Meetings .
• Monitor QMS-related SOPs for effectiveness and revision in line with regulatory requirements and process changes.
  
  

• Knowledge of Quality Management Systems (QMS)
• Good understanding of Change Control & Deviation Management
• Knowledge of GMP / Pharmaceutical Quality Systems
• Working knowledge of SAP
• Good analytical and documentation skills
• Strong follow-up and coordination skills
• Good communication and presentation skills
  
  

• B.Pharm / M.Pharm / B.Sc. / M.Sc. or relevant qualification
• Experience in Quality Assurance / QMS in the pharmaceutical industry
• Experience in handling Change Control, Deviations, SOPs, Rejections and Quality Reviews preferred
• Location: Pawane, Navi Mumbai