Roles Overview

Aspiro Pharma is hiring experienced professionals for sterile injectable manufacturing operations, quality management systems, lyophilization engineering, instrumentation, and quality assurance validation activities for its USFDA-approved injectable facility

Job Responsibilities

Production – Vial Filling & QMS

– Aseptic vial filling operations
– Machine setup and operation
– Line clearance
– IPC activities
– Equipment cleaning
– cGMP compliance
– GDP documentation
– Sterile manufacturing operations

Production QMS

– Deviation management
– Change control
– CAPA implementation
– SOP preparation
– Batch record review
– Risk assessment
– Data integrity (ALCOA+)
– Regulatory audit support

Engineering

– Lyophilizer operation
– CIP/SIP activities
– Loading and unloading
– Recipe management
– SCADA/HMI operations
– Instrument calibration
– PLC troubleshooting
– Preventive maintenance
– Utility coordination

Key Deliverables

• Ensure sterile manufacturing compliance
• Maintain cGMP/GDP standards
• Support regulatory inspections
• Execute validation protocols
• Maintain accurate documentation
• Ensure data integrity (ALCOA+)
• Improve operational efficiency

Important Notes

• Experience required: 2-8 years.
• Sterile injectable manufacturing experience preferred.
• Bring updated resume and salary documents.
• Regulatory knowledge (USFDA/MHRA/EU GMP) is preferred.
• Candidates unable to attend may email their CV to Email ID: naresh.e@aspiropharma.com

How to Apply

• Attend the interview directly at the venue on the scheduled Date: 28 June 2026, Time: 10:00 AM to 03:00 PM
• Carry the following documents:
– Updated Resume
– Last 3 months Payslips
– Bank Statement
– Current CTC Annexure
– Educational Certificates
– Government ID Proof