krg technology inc
Senior Project Manager
krg technology inc, Waco, Texas, United States, 76796
10 - 12 Yrs IT experience which includes 7 - 8 yrs in PharmaResponsibilities
Developing RFP, reviewing responses, and selecting vendors.Facility monitoring system design.Driving all Risk Assessments, Functional Specifications, and Validation efforts.Understanding Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.Applying Project Management / Planning practices, principles, tools, and techniques.Implementing pharmaceutical industry practices and principles including environmental monitoring systems.Adhering to company policies and procedures, including personnel and safety rules and regulations.Experience in a pharmaceutical manufacturing environment preferred, including GMP, Facilities, and Manufacturing equipment.Knowledge of cleanroom monitoring including but not limited to viable air sampling, total particulate sampling, viable surface sampling, pressure differential monitoring, and temperature & humidity monitoring.Knowledge of aseptic cleanroom environments.Additional Information
10 - 12 Yrs IT experience which includes 7 - 8 yrs in PharmaUnderstanding Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
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Developing RFP, reviewing responses, and selecting vendors.Facility monitoring system design.Driving all Risk Assessments, Functional Specifications, and Validation efforts.Understanding Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.Applying Project Management / Planning practices, principles, tools, and techniques.Implementing pharmaceutical industry practices and principles including environmental monitoring systems.Adhering to company policies and procedures, including personnel and safety rules and regulations.Experience in a pharmaceutical manufacturing environment preferred, including GMP, Facilities, and Manufacturing equipment.Knowledge of cleanroom monitoring including but not limited to viable air sampling, total particulate sampling, viable surface sampling, pressure differential monitoring, and temperature & humidity monitoring.Knowledge of aseptic cleanroom environments.Additional Information
10 - 12 Yrs IT experience which includes 7 - 8 yrs in PharmaUnderstanding Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
#J-18808-Ljbffr