Review and approve manufacturing documentation, including batch records and standard operating procedures (SOPs), to ensure compliance with regulatory requirements and internal quality standards.

Conduct regular audits of pharmaceutical manufacturing facilities to verify adherence to Good Manufacturing Practices (GMP) and other relevant regulations.

Oversee the testing and analysis of raw materials, in-process samples, and finished products to ensure they meet established quality specifications and regulatory standards.

Manage and investigate product complaints, deviations, and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA) to address root causes.

Develop and implement quality control procedures and systems to monitor and maintain the quality of pharmaceutical products throughout their lifecycle.

Collaborate with cross-functional teams, including manufacturing, research and development, and regulatory affairs, to ensure quality considerations are integrated into all aspects of pharmaceutical operations.

Stay updated with current regulatory requirements and industry standards, such as those set by CDSCO, WHO, and other relevant agencies, to ensure ongoing compliance.

Provide training and guidance to pharmaceutical staff on quality assurance principles, GMP requirements, and standard operating procedures.

Participate in the validation and qualification of equipment, processes, and analytical methods to ensure their reliability and accuracy.

Manage the stability testing program for pharmaceutical products to determine their shelf life and storage conditions.

Prepare and review quality documentation for regulatory submissions, such as drug master files (DMFs) and new drug applications (NDAs).

Routinely review medication charts for accuracy and potential interactions.

Conduct regular audits of pharmaceutical processes and documentation.

Develop and update Standard Operating Procedures (SOPs) for pharmacy practices.

Ensure compliance with all applicable pharmaceutical regulations and guidelines.

Identify and mitigate potential risks in pharmaceutical compounding and dispensing.

Train pharmacy staff on quality assurance procedures and best practices.

Manage and report adverse drug events according to regulatory requirements.

Implement continuous improvement initiatives to enhance pharmacy quality.

Oversee the validation and calibration of pharmaceutical equipment.

Analyze quality data to identify trends and areas for improvement.

Qualify and monitor pharmaceutical vendors to ensure quality standards.