We are looking for 3 to 4 years experience person in pharma QC department. If interested please contact us.
Responsibilities :
• Conduct quality control testing and inspections on pharmaceutical raw materials, intermediate products, and finished goods according to established procedures.
• Ensure compliance with regulatory requirements, industry standards, and company quality control protocols.
• Maintain and calibrate laboratory equipment and instruments as needed to ensure accurate testing results.
• Document and report any deviations, out-of-specification results, or quality issues promptly, and collaborate with the Quality team to address and resolve them.
• Assist in the validation and qualification of analytical methods and testing procedures.
• Perform data analysis, interpretation, and documentation of test results with a high level of accuracy.
• Monitor and maintain good laboratory practices (GLP) and good manufacturing practices (GMP) in the QC laboratory.
• Support investigations, root cause analysis, and corrective and preventive actions (CAPA) related to quality issues.
• Participate in the training of QC technicians and contribute to the continuous improvement of QC processes.
• Ensure that all quality control records and documentation are complete, organized, and in compliance with relevant standards.
Skills:
• Strong knowledge of pharmaceutical quality control practices, GMP, and GLP, RM, BP, FP, HPLC, etc.
• Proficiency in analytical techniques, instrumentation, and laboratory procedures.
• Excellent attention to detail and analytical skills.
• Ability to work independently and as part of a team.
• Understanding of regulatory guidelines and quality standards in the pharmaceutical sector