Technical Writer with 8 years of experience in a highly regulated Class III PMA and 510k medical device manufacturing environment. Over 9 years of experience developing content for lay users, ALS/BLS users, test engineers, training and implementation coordinators. Enthusiastic about usability and writing to improve the User Experience.
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To support the project timeline, which included approval from the FDA, a one page supplement was create per language and added to each Operating Instruction shipment.
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