Must have a Bachelors degree or foreign equivalent in Chemical Engineering, Biological Engineering or a related field plus four 4 years of experience in the position offered, as a Process Engineer or in a related position. Must have four 4 years of experience in the pharmaceutical production sector with each of the following Conducting technology transfers and commercial support of complex oral solid dosage form unit operations in top spray fluid bed granulation, wet granulation, roller compaction, bilayer compression, or multitip tablet compression; Implementing continuous improvement and capacity improvement projects within oral solid dosage form manufacturing processes; Designing and executing process qualifications and validations required when implementing improvements; Problem solving and issue investigation using structured problem solving methodologies including DMAIC, PPS, or KepnerTregoe; Performing data visualization, data analysis, and data interpretation using statistical software including Minitab, JMP, SAS, or R; Conducting Continued Process Verification for commercial product support in understanding the underlying relationships between raw materials, process parameters, and final critical quality attributes; and Extracting and interpreting data from source systems including SAP, LIMs, PASX, OSIPI, or Manufacturing Data Historians. In the alternative, Employer will accept a Masters degree in Chemical Engineering, Biological Engineering or a related field plus one 1 year of experience. Employer will accept pre or post MA degree experience. Any combination of education, experience or training is acceptable.
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