Multiple openings. Lead inspection & ops quality engineering teams for medical devices. Design, implement, & maintain QA procedures & work instructions to ensure external safety, quality, & compliance w/ company standards & government regulations. Supervise QA engineers. 25% domestic & international travel required.
Requirements: Master's or foreign equivalent in Industrial Engineering, Mechanical Engineering, or related engineering field & 2 years' experience in position offered or related, including 2 years' experience with: Medical devices & ISO 13485 quality standards; Technical writing for QA activities & best practices; Mechanical inspection & inspection equipment; Manufacturing processes, including injection molding, metrology, machining, grinding, product cleaning & circuit board manufacturing; Solidworks, Solidworks ePDM, Oracle R12, Agile PLM, PC-DMIS.
Resume to DJO, LLC, a subsidiary of Enovis Corp, to [email protected] & reference job title in subject.
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