B. Pharm / M. Pharm.
Minimum 15 years of experience in Quality Assurance, with expertise in formulation plants and tablet manufacturing.
Key Responsibilities:
Oversee quality assurance processes in the formulation and tablet production unit.
Develop, implement, and maintain QA protocols to ensure compliance with GMP, regulatory requirements, and company standards.
Lead quality audits (internal and external) and prepare the plant for inspections by regulatory authorities.
Coordinate with cross-functional teams (production, R&D, QC) to address quality issues effectively.
Monitor and ensure compliance in documentation, validation, and equipment calibration processes.
Provide training and mentorship to QA staff to maintain high performance and adherence to quality standards.
Handle deviations, CAPAs, and change control systems promptly and efficiently.