Senior Project Manager

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 . Sevagan sevagan at KRG Technologies Inc. 661 367 8000 * 513