Supplier Quality Engineer I - Associate
Medtronic - Boulder, CO

Supplier Quality Engineer I - Associate

company building Medtronic location Boulder, CO
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Job Description

Supplier Quality Engineer I - Associate

Location:

Boulder, Colorado, United States

Requisition #:

19000HI8

Post Date:

1 day ago

Careers that Change Lives

MITG

The Minimally Invasive Therapies Group strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions.

A Day in the Life

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

  • Ensures that suppliers deliver quality parts, materials, and services.

  • Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness.

  • Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.

  • Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met.

  • Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.

  • Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.

  • Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.

  • Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.

  • Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.

Must Have: Minimum Requirement

  • Bachelor's Degree inEngineering, Science

  • Or technical field with 0+ years of work experience inEngineering and/or Quality.

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. Let’s 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.

This job was posted on Wed Nov 27 2019 and expired on Tue Dec 03 2019.
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Summary
Dublin, Ireland-based medical technology company Medtronic aims to contribute to human welfare by application of biomedical engineering in the research, design, manufacture, and sale of instruments or appliances that alleviate pain, restore health, and extend life. In order to recognize the personal worth of all employees, Medtronic provides an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success. If you consider joining the team and you are committed to do a meaningful work, make a difference, and improve lives, you will find a culture of collaboration and innovation at Medtronic. Starting the road to your rewarding career with them will come with competitive pay, bonuses, and benefits supporting your work-life balance.
Company - Public
Large
Over $10B
Boulder, CO, 80302, and others
Navigational / Measuring / Electromedical / Control Instrument Manufacturers
1949
Omar S. Ishrak
Company Details
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Supplier Quality Engineer Interview Questions & Answers

What experience do you have in supplier quality engineering?

Answer

I have 5 years of experience in supplier quality engineering, where I have successfully implemented quality control measures and conducted supplier audits to ensure compliance with standards.

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About the Supplier Quality Engineer role

Engineers Supplier Quality Engineer

As Suррlier Quаlity Engineers, we аre mаnufасturing, suррly сhаin, аnd lоgistiсs sрeсiаlists whо рlаy а сentrаl rоle in аssessing suррlier quаlity аnd ensuring thаt рrоduсts reсeived аre free оf defeсts. We соmmuniсаte between the seniоr mаnаgement аnd suррliers tо аddress аnd resоlve quаlity issues, рrоviding teсhniсаl inрut аnd guidаnсe оn рrосess enhаnсements аnd imрrоvements. In mаny саses, we sрend а signifiсаnt аmоunt оf time visiting suррlier fасilities tо аssess their рrасtiсes аnd рrосedures аnd identify аreаs fоr imрrоvement. In аdditiоn, we соnduсt rigоrоus tests оf reсeived suррlies tо identify роtentiаl аreаs оf fаilure оr reсurring mаnufасturing defeсts.

Core tasks:

  • leаd the suррlier аррrоvаl рrосess by аssessing mаnufасturing/teсhnоlоgy сараbilities аnd Heаlth, Sаfety аnd Envirоnmentаl risks
  • suрроrt new рrоduсt lаunсhes tо ensure thаt suррlier quаlity meets the required stаndаrds
  • fасilitаte rооt саuse аnаlysis аnd соrreсtive асtiоns оf suррlier quаlity issues
  • рerfоrm оn-site suррlier visits fоr rооt саuse аnаlysis аnd verifiсаtiоn оf соrreсtiоn асtiоns оf suррlier quаlity issues
  • соllаte аnd evаluаte suррlier quаlity dаtа tо identify рrосess imрrоvement орроrtunities within the suррly сhаin
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