Masters degree in Biomedical, Mechanical, Industrial, or other Engineering, or a related field, plus two 2 years of experience. Two 2 years of related experience in FDAGMP regulated industry. Any amount of experience in the following Leading functional and crossfunctional teams to achieve project goals; Delivering multidisciplinary projects; Defining problems, collecting data, establishing facts, and drawing valid conclusions; Writing reports, business correspondence and procedure manuals; Design, review, execution, and approval ofbr installation, Operation and Process Qualification protocols and reports IQOQPO. Knowledge in the following AutoCAD, SolidWorks, Minitab, Word, Excel and Project; Manufacturingbr methods, procedures, and cost reductionyield improvement techniques.

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