BS degree in electrical, mechanical, or biomedical engineering or related engineering with minimum of 5 years of relevant experience. Project management experience, ability to influence cross functional global teams spanning quality, operations, R&D, and sourcing. Experience in process validation, design controls, risk management, and CAPA. Ability to work independently; organized and self-driven. Strong communicator, adept at packaging and appropriately scaling information to the intended audience. Domestic and international travel up to 20%. Experience with Capital Equipment or PCBA manufacturing. Experience with acquisition & integration, hybrid quality systems. Experience scaling manufacturing capacity. Experience in medical device and medical device suppliers. Experience as lead auditor of quality systems (ISO13485 or similar) ASQ certification (CQE, CBA, SSGB, SSBB).
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees