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Location

Boulder, CO | United States

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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:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people
  
  

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.

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Job tags

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Salary