General Manager QA

Roles and Responsibilities

• Ensure compliance with USFDA regulations for injectable products (sterile) and solid oral dosage forms.
• Develop, implement, and maintain quality systems to ensure product quality and regulatory compliance.
• Conduct audits of manufacturing facilities, laboratories, and other departments to identify areas for improvement.
• Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
• Provide training on Good Manufacturing Practices (GMP), cGMP guidelines, OSD requirements, sterility testing methods.

Desired Candidate Profile

• M.Pharma/M.Sc from a recognized university with 20-25 years of experience in pharmaceutical industry.
• Strong knowledge of QA/QC principles, USFDA regulations, injectables production processes.
• Experience in auditing procedures; ability to conduct internal audits independently.