Principal Quality Engineer

Job Description

Requirements:

Bachelor's Degree in Mechanical Engineering or equivalent.

10+ years medical device manufacturing industry experience.

Master's degree in Engineering with 8+ years industry experience.

Thorough understanding of medical device manufacturing, especially as it relates to FDA (cGMP) manufacturing requirements.

Domestic and international travel will be required

Knowledgeable of and works within FDA, MDR, ISO, IEC 60601, and other relevant regulations and standards.

Proficient with root cause analysis and corrective/preventive action procedures.

Proficient with statistics.

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction recordsCompany Description

Specializes in custom automation projects, they are a major player in the world of controls and robotic solutions around the world. My client will expand anyone resume and build them to be a top performing controls engineer.