QC Analyst

A leading Pharma is seeking a diligent QC Analyst with a strong background in quality control testing within the pharmaceutical industry. The ideal candidate has three years of experience in performing analytical testing using instrumentation such as HPLC, GC, and UV-Vis. They ensure adherence to Good Manufacturing Practice (GMP) and maintain equipment calibration and qualification standards. This role involves managing a team of three, requiring coordination and oversight to maintain high-quality testing processes and results. The QC Analyst works closely with production and quality assurance teams to monitor and verify product quality. They analyze data meticulously, maintain accurate records, and contribute to continuous improvement initiatives. The candidate must demonstrate attention to detail, problem-solving capabilities, and the ability to lead and mentor team members effectively while ensuring compliance with industry regulations and company standards.

Responsibilities

Perform routine and non-routine quality control testing on raw materials, in-process samples, and finished products using analytical instrumentation including HPLC, GC, and UV-Vis.
Ensure proper calibration, qualification, and maintenance of laboratory equipment to guarantee accurate and reliable test results.
Review and interpret analytical data in accordance with established procedures and regulatory requirements.
Maintain detailed, accurate, and timely documentation of all QC activities, including test results, instrument maintenance, and deviations.
Manage and supervise a team of three QC analysts, providing training, guidance, and performance evaluations to ensure adherence to quality and safety standards.
Implement and uphold Good Manufacturing Practice (GMP) guidelines throughout all testing processes and laboratory operations.
Coordinate with the production and quality assurance departments to support product release decisions by providing validated analytical data.
Investigate and report any discrepancies or non-conformances detected during quality control testing and participate in root cause analysis and corrective actions.
Contribute to the development, review, and updating of standard operating procedures (SOPs) relevant to quality control testing and laboratory operations.
Support internal and external audits by providing necessary documentation, explanations, and corrective action plans as needed.
Promote and participate in continuous improvement initiatives aimed at enhancing laboratory efficiency, accuracy, and compliance.
Ensure a safe and compliant laboratory environment by following all company and regulatory safety protocols.