Quality Engineer | Pleasant Prairie, WI

Description Plan, coordinate, and execute quality control programs ensuring compliance to ISO13485 and FDA standards Investigate and address customer complaints - CAPA Assist with preparing and executing internal and external audits Handle document and process controls Update documentation and data within the QMS Create and direct validations (IQ/OQ/PQ) Create PPAP documentation Profile 5+ years of quality experience in medical device Understanding of ISO13485 and FDA standards Experience with metal fabrication required, CNC preferred GD&T/PPAP experience Knowledge of QMS software and associated document control Certifications a plus Job Offer Salary ranging from $85,000-$100,000 depending on experience 3 weeks of PTO - accrues from day one Full medical benefit plans offered on day one Ancillary benefits Retirement plan with employer match MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. #J-18808-Ljbffr Michael Page