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

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Associate Project Engineer / Device Complaints Support

requirements (e. g. cGMP, 21 CFR 820, ISO 13485, Canadian MDR) Knowledge of complaint handling and quality systems; device... our collective expertise Associate Project Engineer/ Device Compliances Responsibilities: Support handling customer complaints...

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Company: Verista

Location: Indianapolis, IN

Posted Date: 07 Jun 2025

Salary: $80465 - 93278 per year

Device Customer Complaints Investigator / Project Engineer

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...