Position Title: Development Process Engineer
Work Location: St. Paul, MN 55117
Assignment Duration: 12 Months
Key Responsibilities:
Establish processes based on product specifications, evaluate process and design alternatives based on Design for Manufacturability principles, understand principles of Cost of Goods Sold, manage program compliance with Quality Control requirements (i.e. Design Control, Process validation etc.), understand IP issues relative to processes being developed, maintain knowledge of new developments in manufacturing and design technologies, understand work environment issues (i.e. OSHA regulations, etc.), support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements, Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, our organization policies, operating procedures, processes, and task assignments.
Background & Context: Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
Qualification & Experience:
- 3-5 yrs, Validation activities in a medical devices
- Reporting Exp
- CAD exp
- Validation Activities
- Scientific Development Exp
- Medical Device Exp a plus
- Education: Bachelor of Science in Engineering or Technical Field, an equivalent combination of education and work experience
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