Location: Plymouth, MN
Duration: 6+ months
Position Description
Seeking a technical writer who has experience with quality documentation in a medical device and validation environment. The candidates should have experience with at least two of following deliverables: user user-requirement specifications (URS), functional specs. (FS), install verification (IV), operation test protocols (OTP). Min. of 3-5 years’ experience in an engineering and FDA compliance environment.
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