Senior Process Validation Engineer – Medical Devices

A medical device company located in Indiana is seeking a mid-senior level Process Validation Engineer. The role involves developing and executing process validation strategies, ensuring compliance with FDA QSR and ISO 13485 standards. The ideal candidate will have over 5 years of experience in medical device manufacturing validations and strong proficiency in statistical tools and cross-functional collaboration. This position is contract-based and primarily focused on pharmaceutical manufacturing.
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