AQA ( Bulk Drugs / API )

• Monitoring of Quality Control related activities.
• Review of audit trials for laboratory Instruments.
• Review of laboratory instruments qualification and Calibrations.
• Review and Monitoring of Calibrations, Preventive maintenance schedules, working standards management.
• Review & Monitoring of analyst qualifications and schedules, Backup and restoration of analytical data.
• Review of finisher product analysis results and its raw data, certificate of analysis before dispatching the material, BPCRs and equipment cleaning records.
• Review of stability data and schedules, packing and labelling records.
• Should have knowledge on OOS / OOT / CAPA / Risk Assessment.
• Knowledge in Empower and open lab software.
• Knowledge in other software related to UV and IR instruments.

Note: Only Male Candidate Required.