Experience must include 1 12 months experience implementing a CAPA process; 2 12 months experience leading risk management activities using FMEA tool; 3 12 months experience using statistical tools to analyze medical device data to improve product quality and reduce product quality variation; and 4 12 months experience performing reviews of protocols for medical device process validations. Any experience requirements may be met concurrently during the same time period.br br All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, ancestry, military and veteran status, age, sex, sexual orientation, disability, genetic information, marital status or registered domestic partner status in accordance with applicable federal and state laws. We maintain a drugfree workplace and perform preemployment substance abuse testing.
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