knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices required in regulated manufacturing environments. Electrical and mechanical engineering background applied to automated or semi-automated manufacturing systems. knowledge of automation/controls, tooling, fixtures, test method development, equipment qualification, and manufacturing process validation. Minitab, JMP, or equivalent preferred. Lean Manufacturing, Six Sigma, Kaizen, value stream mapping, or other continuous improvement methodologies preferred. Skills project management, communication, technical writing, analytical. Requirements Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. 0-1 years in manufacturing engineering, process engineering, validation engineering, or quality engineering within an FDA-regulated environment.
· Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, o...