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RedBrick Staffing is seeking a technically minded QA/Regulated Documentation Assistant in Irvine, CA to support quality systems and manufacturing documentation in a fast-paced medical device environment.
You will draft and route quality records, assist CAPA investigations, and maintain controlled documents within the eQMS, ensuring compliance with ISO 13485 and FDA regulations. This role offers growth opportunities and on-site collaboration with cross-functional teams in a regulated setting.