Actalent
Location
Boulder, CO | United States
Job description
Description:
Maintain the eQMS and modify procedures and forms to regulatory compliance Internal and external audit preparation, execution and follow up Root cause and corrective/preventative actions, complaints and NCRs Participate in design control and development activities Skills: Quality engineering, iso 13485, capa, medical device Top Skills Details: Quality engineering,iso 13485,capa,medical device Additional Skills & Qualifications: 5+ years in Quality Engineering Medical device experience ISO13485/14971 CAPAs, RCA, NCRs Experience Level: Intermediate Level About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Job tags
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