Medical Device QA Technician - IQA & Process Validation
Pulmonx Corporation
Pulmonx Corporation is seeking a QA Inspector to perform inspections and testing of IQA, in-process, and finished goods, contributing to lot release and V&V. You will generate detailed reports, maintain QA logs, and support MRR workflows in a cGMP environment. Candidate should have at least 5 years of QA inspection experience in medical devices, understanding ISO13485 and FDA QSR/cGMP requirements, and be proficient with Microsoft Office and ERP systems. #J-18808-Ljbffr Pulmonx Corporation
Vacancy posted 3 days ago
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