Reviewing basic and detailed design, supporting commissioning and qualification activities, including URS development, FAT, SAT, DQ, IQ, OQ and PQ
Coordinates with different functions like manufacturing, project engineering team, validation and quality for implementation of changes associated with project
Work independently and/or with Lead engineer to complete the engineering projects within schedule, budget and quality constraints
Key Requirements
Minimum 4-10 years work experience in a Biotech or related pharmaceutical manufacturing environment preferred
Have some design experience in various stage of project cycle.
Experience in handling process equipment (Autoclave, Glove box, CIP Skids etc)
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