Leads and manages critical quality projects
Responsible for CAPAs, and non-conformance reports
Represents quality during process development and improvements
Responsible for developing work instructions and procedures for manufacturing processes.
Responsible for conducting training of manufacturing employees
Responsible for developing process validation protocol and reports
• Undergraduate degree in engineering or sciences. Engineering degree preferred
• Medical Device Experience a must
• Manufacturing Experience a plus
• 3-5 years of experience is ideal
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