Bachelor's in engineering or equivalent.
3+ years of system testing, Integration, test automation or related experience
3+ years of experience in medical devices (capital equipment) or related fields (regulated industry preferred).
Strong written and verbal communications skills
Strong attention to detail
Design verification test development, execution, report generation.
Experience with LabVIEW
Knowledge of product development process and design control from concept to volume production.
Knowledge of quality assurance techniques, practices, ISO and Regulatory (FDA) compliance.
Knowledge of medical device regulations and standards (e.g., IEC 60601-1, EU-MDR, FDA cGMP).
Understanding of ventilator and gas sensing products, applications, and technologies a plus.
Six Sigma (DFSS (Design for Six Sigma)) Green Belt certification with actual project experience a plus.
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