Ensure planned progress with respect to the engineering deliverables for projects, process engineering planning & scheduling, preparation of progress reports, manpower & resource forecasts, and utilize resources effectively & efficiently.
Provide process design & detailed engineering including performing process simulations, design calculations, process optimization, sizing & selection of equipment for projects.
Prepare various engineering deliverables (drawings & documents) such as process flow diagrams, P & I diagram, process datasheets, equipment specifications, cause & effect diagrams, control philosophies, shutdown philosophies, and HAZOP studies & reports.
Facilitates the identification and communication of the root causes of losses in the operation of production equipment and processes.
Provide the necessary process engineering inputs for capex projects to the other disciplines and other departments.
Prepare and issue RFIs, evaluate vendor•s quotations, clarifications, and perform technical bid analysis. Review vendor•s documents, drawings, datasheets, specifications and calculations
Requirements:
Bachelor•s degree in chemical engineering, biochemical engineering, mechanical engineering, or a related field.
At least two years of aseptic pharmaceutical manufacturing/engineering experience.
In depth understanding and application of cGMP principles, concepts, practices and standards.
Must have at least one year of upstream and downstream bulk sterile processing experience and understand the operating principles of bioreactors, chrome skids, and filtration skids working in a pilot plant.