Ensuring adherence to Good Manufacturing Practices (GMP) and quality standards throughout the pharmaceutical production process.

Conducting thorough quality control tests on raw materials, in-process samples, and finished products to verify compliance with specifications.

Analyzing and interpreting quality control data to identify trends, deviations, and potential areas for improvement in manufacturing processes.

Documenting and maintaining accurate records of all quality control activities, test results, and deviations for regulatory compliance.

Investigating and resolving quality-related issues, such as deviations, out-of-specification results, and customer complaints, using root cause analysis.

Collaborating with production, research and development, and regulatory affairs teams to ensure product quality and compliance.

Developing and validating analytical methods for quality control testing, ensuring accuracy, precision, and reliability of results.

Performing regular audits of manufacturing facilities and quality control laboratories to assess compliance with regulatory requirements and internal standards.

Training and mentoring quality control personnel on testing procedures, data analysis, and quality assurance principles.

Reviewing and approving batch production records, ensuring all steps were performed according to standard operating procedures (SOPs).

Managing and maintaining quality control equipment, including calibration, validation, and troubleshooting.

Participating in the development and implementation of quality management systems (QMS) to enhance overall product quality.