<ul><li>Ensure compliance with GMP, WHO, USFDA, MHRA, and other regulatory guidelines.</li><li>Conduct in-process quality checks during manufacturing and packaging.</li><li>Maintain and review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).</li><li>Prepare, update, and implement Standard Operating Procedures (SOPs).</li><li>Ensure proper documentation of deviations, change controls, and validation reports.Identify, investigate, and address quality issues and deviations.</li><li>Monitor the implementation of Corrective and Preventive Actions (CAPA).</li><li>Assist in internal, external, and regulatory audits.</li><li>Ensure compliance with Quality Management Systems (QMS) and Good Laboratory Practices (GLP).</li><li>Support regulatory submissions by providing necessary documentation.</li></ul><p>&nbsp;</p>

QA Executive