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Mahasurya Ventures India is seeking a QA professional to conduct comprehensive QA activities in pharmaceutical manufacturing, ensuring GMP/GDP compliance, IPQA, and line clearance. You will review batch records, deviations, CAPA, and change control to maintain regulatory standards.
The role emphasizes rigorous documentation, investigation, and adherence to SOPs, with involvement in audits and regulatory inspections to uphold product quality and patient safety.
Conduct QA activities for pharmaceutical manufacturing, IPQA, line clearance, batch record review, deviations, CAPA, change control, SOP compliance, GMP, GDP, audits, validation, documentation, investigation & regulatory compliance.
Strong knowledge of GMP, GDP, IPQA, batch documentation, line clearance, CAPA, deviations, change control, SOPs, validation, audits, regulatory compliance, documentation & investigation.