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EPM Scientific in Palo Alto is seeking a Quality Engineer to support design controls across the product lifecycle for next-generation medical devices. You will maintain DHFs, risk management files, and validation activities, ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and ISO 14971. The role collaborates with R&D on design reviews and CAPA, contributing to NPI and commercialization efforts.

Also on the board Same function, level within a rung

Level

Lead

Location

Palo Alto, CA

Occupation

Validation Engineers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

2 days ago

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