1+ months

Sr Supplier Quality Engineer

Medtronic
Irvine, CA 92604
Sr Supplier Quality Engineer

Location:

Irvine, California, United States

Requisition #:

2200079C

Post Date:

May 04, 2022


**Careers That Change Lives**


In this exciting role as a Senior Supplier Quality Engineer, you will have responsibility for and authority to provide Quality Assurance Engineering representation to select business teams facilitating design transfer to manufacturing, and process improvements to obtain optimum product reliability, safety, and effectiveness. Coordinate feedback of quality indicators and statistics to business team for use in business decisions. Partner with Operation quality and site Manufacturing Engineers in process improvements. Perform, direct, or consult in validations. QA approvals for Engineering Change Notices, test methods, and test equipment to assure the design and production of medical devices are following applicable standards. Drive investigations, corrective action implementation, and corrective action verification activities assigned to business teams.


**Vascular Platform**


The Vascular Platform operations 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.


**A Day in the Life**


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


You will establish and successfully execute supplier management plans which will align to overall business objectives.


+ Partners with Site RD, Quality, Manufacturing Engineering to assist in developing test methods, equipment acquisition for new product testing, validations/qualifications, statistical analysis of data for significance, and other documented requirements for quality objectives.

+ Participates in released product engineering projects including select suppliers, qualify new suppliers, and setup supplier controls.

+ Investigates and reports on supplier corrective actions effectiveness and timeliness.

+ Participate on Corporate Supplier Quality Teams.

+ Develop and ensure proper execution of the Supplier Quality Strategy.

+ Manage all Supplier Quality related activities.

+ Partner with Supply Chain to integrate strategies and ensure coordination and alignment across Sector.

+ Assist with supplier development by evaluating and developing supplier processes through process and product and/or tooling validations and provide assistance, conduct supplier review meetings and supplier training.

+ All activities must be performed in compliance with the Quality System.

+ Performs duties in compliance with environmental, health and safety related site rules, policies, or governmental regulations.

+ All other duties as assigned.

+ Travel requirement:less than 25%


**Must Have: Minimum Requirements**


**To be considered for this role, please ensure the minimum requirements are evident on your resume.**


Bachelors degree in Engineering, Science or technical field with 4+years experience in engineering and/or quality OR Advanced degree with 2+ years experience in engineering and/or quality


**Nice to Have**


+ Five or more years experience with a BS degree in engineering or three or more years experience with a Masters degree.

+ Minimum of three years industry experience, preferably in the medical device, Electronic, Automotive, Aerospace or Pharmaceutical.

+ Prior experience with electro-mechanical commodities


+ Bachelors or Masters Degree in Electrical Engineering, or other related engineering degree strongly preferred.

+ Experience in medical device design and application of test standards.

+ Experience in application statistical methods to design reliability and process capability.

+ Certified Quality Engineer, Reliability Engineer, or equivalent desired.

+ Strong oral and written communication skills.

+ Cross-functionally and an effective team player.

+ Excellent presentation skills.

+ Must be able to handle multiple tasks/projects and manage priorities accordingly.

+ Working knowledge of appropriate industry standards.

+ Experience in application statistical methods to design reliability and process capability.

+ Must be able to work in a team environment and exert influence without alienating others.

+ Knowledge/basic understanding of specification development, industry standards, geometric dimensioning and tolerancing (GDT), etc.

+ Knowledge with PPAP process and part/product validation and qualification.


**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 above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.


The physical demands described within the Day in the Life 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.


Travel requirement up to 25% both domestic and international


**EEO**


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.


This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here:http (http://www.uscis.gov/e-verify/employees) :// www.uscis.gov/e-verify/employees
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.

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Posted: 2022-07-01 Expires: 2022-09-01

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Sr Supplier Quality Engineer

Medtronic
Irvine, CA 92604

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