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.

Implementing and maintaining quality assurance procedures to ensure compliance with regulatory standards.

Ensuring adherence to pharmaceutical regulations and guidelines set by Indian regulatory bodies.

Reviewing and approving documentation related to manufacturing, testing, and quality control processes.

Overseeing the release of pharmaceutical batches after thorough quality checks and compliance verification.

Conducting internal audits to identify areas for improvement in quality control processes.

Developing and validating testing protocols for raw materials, in-process samples, and finished products.

Analyzing quality control data to identify trends, deviations, and potential issues.

Ensuring that all quality control equipment is properly calibrated and maintained.

Investigating and resolving deviations from established quality control procedures.

Training quality control staff on standard operating procedures and regulatory requirements.

Evaluating and managing the quality of raw materials and services provided by vendors.

Conducting thorough inspections of pharmaceutical products to ensure they meet quality standards.

Analyzing samples of raw materials and finished products using various laboratory techniques.

Documenting and maintaining detailed records of quality control tests and results.

Identifying and addressing any deviations from established quality control procedures.

Collaborating with production teams to implement corrective actions and prevent future quality issues.

Developing and validating analytical methods for testing pharmaceutical products.

Ensuring compliance with regulatory requirements, such as those set by CDSCO and other relevant agencies.

Participating in audits and inspections conducted by regulatory bodies.

Training and supervising quality control technicians and other staff members.

Reviewing and approving batch records and other documentation to ensure accuracy and completeness.

Managing and maintaining laboratory equipment and instruments.

Staying updated with current good manufacturing practices (cGMP) and other industry standards.

Investigating and resolving customer complaints related to product quality.

Implementing and monitoring quality control systems and procedures.

Contributing to the development and improvement of quality control processes.