Medtronic Irvine, CA is seeking a Tech comm Specialist/ Writer to develop labeling and regulatory documentation for Neurovascular products. You will define labeling strategy, manage translation, and oversee PLM changes while ensuring compliance with 21 CFR, EU MDR, ISO standards and Medtronic quality systems.
The role requires at least 2 years in regulatory/product compliance, labeling, or technical writing in medical devices, with strong written communication skills and the ability to work
#J-18808-LjbffrRegulatory Tech Writer & Labeling Designer in irvine at Unknown Company
This position is listed as full time and onsite.