Daisy Ramirez

Production Supervisor at Bora Pharmaceuticals

Based in Mississauga, Canada

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Seniority

Manager

Department

Manufacturing & Production

Location

Mississauga

Industry

Pharmaceutical Manufacturing

Company size

682

Contact information

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Email

1 credit

d•••••••@boracorpcdmo.com

Phone

5 credits

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Background

About Daisy Ramirez

PROFESSIONAL EXPERIENCE: Subject Matter Expert - Packaging/ Aseptic Filling/Process Control Operator 1) Performed product quality checks at various points of the production run. 2) Effectively audited batch records and log books to ensure all documentation was completed using GDP techniques. 3) Performed production line approval and line clearance verifications. 4) Operated computerized and manual equipment for production processes, meeting specification. 5) Prepared and revised production documents such as Standard Operating Procedure, manufacturing batch record, inventory reports and productivity reports providing up to date information. 6) Ensured that productivity is maintained and that neither quality or safety is compromised. 7) Sent daily updates to the department; as well as microbiology and chemistry samples to the microbiology and chemistry lab. 8) Performed troubleshooting with issues in filling and packaging lines, ensuring resolution prior to and during production. 9) Actively reviewed Environmental Monitoring System (Insight) for alarms and respond with appropriate corrective measures, and prepared all required quality documentation. 10) Conducted On the job training and Performance Observation for Packaging and Process Control Operator, increasing the employees skills and ensuring that GDP's and SOP's were followed. 11) Performed Daily Environmental Monitoring of the cleanroom on behalf of the Microbiology Department; which include surface, air and particulate testing, following the proper aseptic techniques. 12) Successfully performed role as a Filling Operator by paying strict adherence to the sanitization and disinfection program for the filling area. 13) Transferred and dispensed product components into the sterile rooms using proper aseptic techniques. 14) Issued Non Scheduled Work Orders as per production and safety needs. 15) Initiated Non-Conformance Reports (NCR), ensuring accuracy of information for corrective action.

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