Applicants must have demonstrated experience in the followingbr Process development in medical device or other regulated FDA or QSR and ISO environment;br A regulated manufacturing environment and process validation IQ, OQ, and PQ;br DOE and other statistical methods;br cGMP and GLP;br Analyzing data, interpreting results, and writing reports;br Design and technology transfers;br Creating and execute project plan;br LEAN, Six Sigma or Design for Six Sigma; andbr Basic tooling, design, and drafting.

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