Fortive is seeking a Quality Engineering professional to lead risk management, reviews of design verification and validation, and CAPA coordination within NPI and product life cycle management. The role emphasizes adherence to FDA QSR 21 CFR 820 and ISO13485, with strong cross-functional interaction across R&D, operations, and quality teams. Applicants should have a technical degree and 3–4+ years in quality engineering within regulated industries, plus proficiency in Excel/Office tools and data

Also on the board Same function, level within a rung

Level

Manager

Location

Irvine, CA

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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