Quality Engineer

Medical Devices Company
Andover, MA

Roles & Responsibilities

Description:

Quality Engineer Role
***Looking for Class II Medical Device experience performing Design Transfer activities per FDA CFR 820. Primary responsibilities will be Test Method Validations, Analysis with Minitab Software, IQ/OQ/PQ, Non-Product Software Validation, PFMEA, DFMEA, in accordance with ISO 14971, ISO 13485.

Experience Required

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Skills & Certifications

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Eligibilities & qualifications

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Posted 2026-06-24

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