(QA) IPQA-Manager

KeyBiz Dashboards Pvt Ltd; Hyderabad; On-site; INR 400,000 - 600,000; Full time

Job summary

KeyBiz Dashboards Pvt Ltd in Hyderabad is seeking a Quality Assurance professional to oversee IPQA activities across dispensing, manufacturing, and packing. The role involves ensuring compliance with GMP guidelines and conducting training for shop-floor personnel on GMP compliance.

The ideal candidate will manage critical processes and monitor deviations while supporting audits and inspections. Proficiency in documentation practices and collaboration with various teams is essential for this position.

Responsibilities

• Oversee IPQA activities across production areas including dispensing, manufacturing, and packing.
• Ensure real-time monitoring of manufacturing processes as per GMP and approved SOPs.
• Perform line clearance activities before and during production operations.
• Review and ensure compliance of batch manufacturing records (BMR) and batch packaging records (BPR).
• Monitor critical process parameters and ensure adherence to validated processes.
• Handle deviations, investigations, CAPA, and change control related to production activities.
• Conduct shop-floor audits and ensure compliance with GMP, GDP, and data integrity requirements.
• Coordinate with Production, QC, Engineering, and Regulatory teams for quality-related activities.
• Ensure proper documentation practices are followed across manufacturing areas.
• Support internal audits, regulatory inspections (USFDA, WHO, EU GMP), and client audits.
• Train and guide IPQA executives and shop-floor personnel on GMP compliance.
• Ensure timely reporting and escalation of quality issues to management.

Job description

• Oversee IPQA activities across production areas including dispensing, manufacturing, and packing.
• Ensure real-time monitoring of manufacturing processes as per GMP and approved SOPs.
• Perform line clearance activities before and during production operations.
• Review and ensure compliance of batch manufacturing records (BMR) and batch packaging records (BPR).
• Monitor critical process parameters and ensure adherence to validated processes.
• Handle deviations, investigations, CAPA, and change control related to production activities.
• Conduct shop-floor audits and ensure compliance with GMP, GDP, and data integrity requirements.
• Coordinate with Production, QC, Engineering, and Regulatory teams for quality-related activities.
• Ensure proper documentation practices are followed across manufacturing areas.
• Support internal audits, regulatory inspections (USFDA, WHO, EU GMP), and client audits.
• Train and guide IPQA executives and shop-floor personnel on GMP compliance.
• Ensure timely reporting and escalation of quality issues to management.