Key Responsibilities:
Perform equipment, utility, and process validation/qualification activities.
Execute IPQA activities and ensure compliance with GMP and SOPs.
Manage vendor qualification and maintain related documentation.
Handle issuance of batch manufacturing/packing records and other QA documents.
Maintain QA documentation and support audits, inspections, and quality compliance.
Requirements:
B.Pharm/M.Pharm/M.Sc. with 1–3 years of experience in Quality Assurance.
Hands-on experience in validation, qualification, IPQA, vendor management, and document issuance.
Positive knowledge of GMP, GDP, and pharmaceutical quality systems.