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Gregory Lovick previously worked as Process Technician at Biomerieux and Training Coordinator at Biomerieux.
Gregory Lovick is a professional in their field.
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Assists with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns.Assists with the execution of validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state.Provides assistance with the review and.
Carried out new employee orientation and provided training on use of the employee learning portalInstructed various training classes for the manufacturing/production employeesManage the addition and removal of designated training for employeesMaintained and updated the training records for 400 employeesProvided support and assistance to users having.
Assists with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns.Assists with the execution of validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state.Provides assistance with the review and.
Complies with cGMP through adherence to SOP's, Master Batch Record Instructions, and company policies with a focus on quality and safety to produce parenteral products that improve the public health. Ensure training is in compliance with job role before performing any activities in the production operation.
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Gregory Lovick is based in United States, United States, United States.
Gregory Lovick has worked for Biomerieux and App Pharmaceutical.
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