Methode Electronics Inc. is seeking a dynamic individual for a position as Medical Device Quality Assurance and Regulatory Affairs Manager for its Dabir Surfaces Inc. (The “Company”) business unit. Methode Electronics is a global developer of custom engineered and application specific products and solutions with headquarters in the Chicago, IL area. With over 5,500 employees, Methode is financially strong and extremely well positioned to grow from their existing $1.1 billion revenue. Our focus is on design, development and manufacture of solutions for customer applications utilizing our technical capabilities in the areas of power distribution, sensors, human-to-machine interface. Further information can be found at Methode’s website: www.methode.com. www.dabir-surfaces.com
Lead and insure that the company follows all Good Manufacturing Practices and SOP’s as defined by the Company policies, practices and procedures to insure that FDA, European Medical Device Directive, Canadian Medical Device regulations, ISO regulations and the Company quality standards are met.
Methode Electronics is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, genetic information and other legally protected characteristics. The EEO is the Law poster is available here: EEO Poster, if you need a reasonable accommodation because of a disability for any part of the employment process, please send an e-mail to firstname.lastname@example.org or call (708) 867-6777 and let us know the nature of your request and your contact information.