Devi Autar Email & Phone Number | Sep 1990 - 2006 - 16 years of Pharmaceutical Industry Experience as Filling Technician - 2006 - Present - Filling Team Leader - Current Training in GMP and SOP Requirements - Demonstrated knowledge of all aspects of Filling, Washing & Sterilization, Capping and Examination Machines - Assist and Qualify Technicians with Aseptic Process Simulation Validation Study - Review APSS Validation Study Protocol (Aseptic Process Simulation Study) - Support Batch Production Record Simplification - Review Filling Batch Production Records - Perform Environmental Monitoring ISO Certification - Review Rapid Pharma FMS (Facility Management System) - Support Audit Questions for FDA Inspection - Trained Operational Staff as Part of Process Updates - Qualify New Technicians for Personal TSB - Perform RABS Glove Semi-Automated Integrity Test - Perform Environmental Monitoring for Viable and Non-viable Samples - Review Master, MODA-FDC and MODA-EM System for Viable and Non-viable EM Samples - Perform Verification for Non-viable Environmental Monitoring Particulate Samplers - Perform Filter Integrity Test Audit Trail - Cross Functional Team Leadership Skills - Support Investigation for Deviations - Knowledge and Perform S/4 HANA iShift Transactions

Devi Autar

Sep 1990 - 2006 - 16 years of Pharmaceutical Industry Experience as Filling Technician - 2006 - Pre...
Toronto, Toronto, Canada

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Devi Autar’s Location Toronto, Toronto, Canada

Devi Autar’s Current Industry Sanofi Pasteur

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Team Leader

1990-09-01 00:00:00 - Present

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Devi Autar is a Sep 1990 - 2006 - 16 years of Pharmaceutical Industry Experience as Filling Technician - 2006 - Present - Filling Team Leader - Current Training in GMP and SOP Requirements - Demonstrated knowledge of all aspects of Filling, Washing & Sterilization, Capping and Examination Machines - Assist and Qualify Technicians with Aseptic Process Simulation Validation Study - Review APSS Validation Study Protocol (Aseptic Process Simulation Study) - Support Batch Production Record Simplification - Review Filling Batch Production Records - Perform Environmental Monitoring ISO Certification - Review Rapid Pharma FMS (Facility Management System) - Support Audit Questions for FDA Inspection - Trained Operational Staff as Part of Process Updates - Qualify New Technicians for Personal TSB - Perform RABS Glove Semi-Automated Integrity Test - Perform Environmental Monitoring for Viable and Non-viable Samples - Review Master, MODA-FDC and MODA-EM System for Viable and Non-viable EM Samples - Perform Verification for Non-viable Environmental Monitoring Particulate Samplers - Perform Filter Integrity Test Audit Trail - Cross Functional Team Leadership Skills - Support Investigation for Deviations - Knowledge and Perform S/4 HANA iShift Transactions - Create Work Orders