Quick overview
Job description
Sevagan
sevagan at krgtech.com
KRG Technologies Inc.
661 367 8000 * 513
10 -12 Yrs IT exp which includes 7-8 yrs in Pharma
· Developing RFP, review responses and selecting vendor.
· Facility monitoring system design.
· Driving all Risk Assessments, Functional Specifications and Validation efforts.
· Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
· Project Management / Planning practices, principles, tools and techniques.
· Pharmaceutical industry practices and principles including environmental monitoring systems.
· 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.
Client - HCL America Inc
10 -12 Yrs IT exp which includes 7-8 yrs in Pharma
· Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
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