• Handling QA activities as per GMP / WHO-GMP / Schedule M
• BMR/BPR review and documentation
• Line clearance and in-process verification
• Deviation, CAPA & Change Control handling
• SOP preparation, implementation & document control
• GMP/GDP compliance and self-inspection
• Support during regulatory/customer audits
• Validation & qualification documentation
• Coordination with Production, QC, Warehouse & other departments
• Ensure compliance with Quality Management System
? Candidate Profile:
• 5–6 years of relevant experience in Pharmaceutical QA
• Strong knowledge of GMP, WHO-GMP & Schedule M
• Good experience in BMR/BPR review and QA documentation
• Knowledge of Deviation, CAPA, Change Control & Audit handling
• Positive communication and coordination skills
• Experience in pharmaceutical manufacturing preferred
📌 QA EXECUTIVE (India)
🏢 Medella Softgel
📍 India
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