Responsible for overall Quality Assurance and Quality Control operations in the pharmaceutical manufacturing unit and ensuring compliance with GMP, WHO-GMP, and company quality standards.
Key Responsibilities
Manage QA and QC activities.
Ensure GMP and regulatory compliance.
Approve SOPs, BMR/BPR, specifications, and quality documents.
Handle deviations, CAPA, OOS, audits, and inspections.
Monitor in-process quality and batch release.
Ensure training and implementation of quality systems.
Drive continuous quality improvement initiatives.