Quality Assurance - Officer / Sr. Officer

Roles & Responsibilities
• Perform IPQA (In-Process Quality Assurance) activities for dispensing, manufacturing, and packaging operations
• Monitor sterile ophthalmic production processes to ensure GMP compliance
• Conduct in-process checks and line clearances in sterile areas
• Ensure adherence to SOPs, BMR/BPR review, and documentation practices
• Identify deviations and support CAPA implementation
• Coordinate with Production, QC, and Engineering teams for quality compliance
• Participate in audits and regulatory inspections as required
• Maintain quality records and ensure data integrity

Qualification
• B.Pharm (Bachelor of Pharmacy) or M.Pharm (Master of Pharmacy)

Experience
• 3–8 years of experience in Quality Assurance
• Experience in sterile ophthalmic manufacturing preferred

Skills
• Strong knowledge of IPQA activities in sterile manufacturing
• Understanding of GMP and regulatory compliance requirements
• Experience in dispensing, manufacturing, and packaging quality oversight
• Good documentation and investigation handling skills
• Attention to detail and strong analytical ability

About the Company
Ajanta Pharma is a leading Indian pharmaceutical company engaged in the development, manufacturing, and marketing of specialty pharmaceutical formulations, with a strong presence in regulated and emerging markets worldwide.