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Keywords: Associate - QA, Medical Devices Quality Systems and Regulatory Compliance, Location: Indianapolis, IN

Page: 1

Device Customer Complaints Investigator / Quality Specialist

requirements (e. g. cGMP, 21 CFR 820, ISO 13485, Canadian MDR) Knowledge of complaint handling and quality systems; device... include: Support timely completion of product complaint investigations, in compliance with global and local procedures...

Company: Verista
Location: Indianapolis, IN
Posted Date: 30 May 2025
Salary: $80465 - 93278 per year