Sr Design Quality Engineer
Medtronic Inc.
Los Angeles, CA
Full-time
Engineering
Posted on October 27, 2019
Medtronic Inc. Sr. Design Quality Engineer Sr. Design Quality Engineer for Medtronic, Inc. at its facilities located in Northridge, CA. Duties: Participates in the execution of new product development and sustaining products and administration of quality assurance programs, policies, processes, procedures and controls in compliance with the evolving and complex U.S. and global requirements of the medical device industry. Requires a Masters’ Degree in Biomedical Engineering or closely related engineering field and 2 years’ experience in quality engineering in the medical device industry and 2 years post-bachelor’s progressive experience in all of the following: Quality engineering support for the development and V&V (verification and validation) activities; Risk activities to include system risk analysis, DFMEA and PFMEA; Design controls applicable to Medical Device development; Navigating ISO 13485, ISO 14971, FDA 21 CFR 820, IEC 60601-1 and MDD; Working on internationally certified quality systems, USFDA Quality System Regulation; Problem solving, and statistical methods as applied to process and product quality, product development process, root cause analysis, and CAPA. Writing technical reports, business correspondence, technical and administrative procedures. Incidental Travel. Apply at www.medtronic.com/careers, Req.19000KEF. Medtronic is an equal opportunity employer committed to cultural diversity in the workplace. All individuals are encouraged to apply.