Job Summary

　　The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes.

　　Essential Functions

　　Design, review and execute validation document activities such as Factory acceptance test (FAT), Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment /utilities/facilities and generate reports which summarize results, specification and its acceptance criteria

　　Performs re-qualification of equipment, facility and utilities as required

　　Responsible for creating validation project and validation progress reports - weekly and monthly

　　Participate in evaluation of failures and out of specification results impacting compliance with quality, safety and other design requirements

　　Provide Technical Inputs and develop strategy for various domestic and international Site Transfer projects. Provide regular status updates to the department and program management.

　　Closely works with the maintenance & facility teams to complete new equipment installation, commission and validation as per project requirement.

　　Performs engineering assessment and writes investigation reports for non-conformance

　　Additional Responsibilities

　　Assists with engineering projects and performs other duties as assigned.