Conducting rigorous analysis of pharmaceutical raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements.

Performing various chemical tests, including titrations, chromatography (HPLC, GC), spectroscopy (UV-Vis, IR), and other analytical techniques, to determine the identity, purity, and potency of pharmaceutical substances.

Documenting all testing activities, observations, and results accurately and meticulously in laboratory notebooks, batch records, and electronic data management systems, adhering to Good Documentation Practices (GDP).

Evaluating analytical data, identifying trends, and investigating out-of-specification (OOS) results to determine root causes and implement corrective and preventive actions (CAPA).

Maintaining and calibrating laboratory equipment, such as HPLC systems, spectrophotometers, and titrators, to ensure accurate and reliable analytical results.

Participating in method validation and transfer activities to ensure the accuracy, reliability, and reproducibility of analytical methods across different laboratories and instruments.

Reviewing and approving analytical data, test results, and certificates of analysis (COAs) to ensure compliance with quality standards and regulatory requirements.

Collaborating with other departments, such as manufacturing, research and development, and regulatory affairs, to address quality-related issues and support product development activities.

Participating in internal and external audits to assess the effectiveness of the quality control system and identify areas for improvement.

Maintaining inventory of laboratory supplies and reagents, and ensuring proper storage and handling of chemicals and reference standards.

Following safety procedures and guidelines to ensure a safe working environment in the laboratory, including the proper handling and disposal of hazardous materials.

Perform rigorous analytical testing of pharmaceutical raw materials and finished products.

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

Review and approve quality control documentation, including test methods and specifications.

Calibrate and maintain laboratory instruments to ensure accurate and reliable results.

Validate analytical methods to ensure they are accurate, precise, and reliable for intended use.

Conduct stability testing of pharmaceutical products to determine shelf life and storage conditions.

Ensure compliance with standard operating procedures (SOPs) and regulatory requirements.

Investigate deviations from quality control procedures and implement corrective actions.

Participate in internal and external audits to ensure compliance with quality standards.

Conduct training programs for quality control personnel on testing procedures and equipment.

Manage the receipt, storage, and disposal of quality control samples.