• Perform line clearance activities for aseptic and injectable operations
• Monitor washing, filling, sealing, and visual inspection processes
• Conduct environmental monitoring in Grade A, B, C & D cleanrooms
• Ensure compliance with GMP, SOPs, and regulatory requirements
• Support batch documentation, deviations, and investigations
• Coordinate with production and quality teams to maintain compliance
• Monitor aseptic area operations for injectable manufacturing
• Perform and support environmental monitoring and media fill activities
• Handle infusion and solution preparation processes
• Operate and monitor lyophilization, BFS, and injectable bag filling
• Ensure adherence to GMP, safety standards, and SOPs
• Maintain batch records and support process improvements
• QA (IPQA): B.Pharm / M.Pharm
• Production: B.Pharm
• QA (IPQA): 1 – 3 years
• Production: 2 – 9 years
• Aseptic operations & injectable manufacturing
• Cleanroom practices & environmental monitoring
• Lyophilizer, BFS, infusion & solution preparation
• GMP, SOP, and regulatory compliance
• Good documentation and teamwork skills
Date: Sunday, 25th January 2026
Time: 10:00 AM – 3:00 PM
Venue: Aurobindo Pharma Ltd, Unit-III,
Bhachupally, Hyderabad, Telangana
(Selected candidates will be deployed at Eugia Pharma Specialities Ltd.,
Unit-III, Pashamylaram, Patancheru, Sangareddy, Telangana)
Eugia Pharma Specialities Limited, a part of the Aurobindo Pharma Group, is a leading pharmaceutical company focused on injectable formulations and specialty generics. The company is known for its strong presence in regulated markets, advanced aseptic manufacturing capabilities, and commitment to quality, compliance, and innovation. Eugia continues to expand its global footprint while delivering high-quality parenteral products to meet critical healthcare needs worldwide.
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