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1+ months

Design Quality Engineer II - Test Method Validation

Irvine, CA 92604
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Design Quality Engineer II - Test Method Validation


Irvine, California, United States

Requisition #:


Post Date:

Jul 21, 2020

**Careers That ChangeLives**

In this exciting role as
a **Design Quality Engineer II - Test Method Validation,** you will
have primary focus on supporting new product development and test method
validation for the Neurovascular business within the Brain Therapies Group. As
a member of the Design Assurance Engineering team, you will have primary
responsibility for influencing product quality and reliability outcomes across
new product development projects.

The **RestorativeTherapies Group** develops life-restoring therapies and healthcare
solutions that span the care continuum; integrating technologies and applying
clinical and economic evidence to increase patient access, improve efficiency
of procedures and deliver successful patient outcomes.

**BRAIN THERAPIES** offer an integrated portfolio of devices and
therapies for the treatment of neurological disorders and diseases, as well as
surgical technologies designed to improve the precision and workflow of neuro

**A Day in the Life**

Responsibilities may
include the following and other duties may be assigned.

+ Actively represent Quality Engineering function on productdevelopment teams for Test Method Validation

+ Mentor less senior Quality Engineers and technicians

+ Apply knowledge of Design Control principles and qualityengineering to positively influence new product development efforts, includingthose for Voice of the Customer, establishing design inputs/outputs, DesignVerification Validation, Process Characterization Validation,Component Qualification, and Risk Management.

+ Hands on participant in early stages of product developmentincluding but not limited to physician interaction, component engineering,competitive product and prototype testing.

+ Identifies quality characteristics and validation criteria forcomponents, subassemblies, and finished devices.

+ Ensure product development activities are conducted in accordancewith FDA, QSR, ISO 13485 and internal Quality System requirements.

+ Drive predictive engineering methodology principles (DRM)incorporating reliability and capability analysis assessments in Design andManufacturing processes.

+ Travel less than 25%

**Must Have: MinimumRequirements**

Degree in Engineering, Science or technical field with 2+ years of work
experience in Engineering and/or Quality OR Advanced Degree in Engineering,
Science or technical field with 0+ years of work experience in Engineering
and/or Quality

**Nice to Have: Preferred Requirements**

+ Experience with test method validation including destructive andnon-destructive variable RR, Type 1 and Attribute studies.

+ Experience with vascular devices, embolic coils, stents and/orcatheters

+ Design, Reliability and Manufacturability (DRM) and/or Design forSix Sigma (DFSS)

+ Experience with Risk Management

+ Self-motivated, driven and committed to a team approach

+ Strong interpersonal, organizational and project management skills

+ Strong oral, presentation and technical writing skills

**About Medtronic**

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.

Physical Job Requirements

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


Posted: 2020-07-23 Expires: 2020-09-28
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Design Quality Engineer II - Test Method Validation

Irvine, CA 92604

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