Katalyst HealthCares and Life Sciences in Santa Clara, CA is seeking a Medical Device & Regulations Engineer to develop and maintain software QA processes for non-product software used in medical device development. You will ensure compliance with FDA, ISO 13485, IEC 62304, support audits, validate computerized systems, and collaborate with software development and IT teams to strengthen quality practices.

Also on the board Same function, level within a rung

Level

Lead

Location

Santa Clara, CA

Occupation

Validation Engineers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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