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Quality Engineer

Medtronic


Location:
Fourmies
Date:
05/17/2018
2018-05-172018-06-16
Job Code:
34956
Categories:
  • Engineering
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Job Details

Company Medtronic
Job Title Quality Engineer
JobId 34956
Location: Fourmies, FRA

Description
Quality Engineer

Location:

Fourmies, Nord-Pas-de-Calais, France

Requisition #:

17000ITL

Post Date:

Oct 10, 2017

**Careers that change lives !**

To be the lead in the supplier management processes as applicable within the Medtronic Structural Heart Operations facility in Medtronic Fabrication, Fourmies (59) to ensure compliance against the corporate supplier management policies, as well as applicable regulatory regulations. To drive the facilities suppliers towards MDT Operational Standards by developing their ability to deliver quality parts and services, through the application of effective preventative and problem solving techniques, as well as ensuring a flawless manufacturing process through appropriate quality planning.

You will work in close cooperation with all the facilities departments, as well as the corporate quality supplier engineer group to which you will functionally report.

**Your mission**

+ Support the vendor and customer complaint handling process;

+ Supporting the teams in Medtronic Fabrication, Fourmies (59) in the selection, support and evaluation of global best-in-class third party suppliers;

+ Communicating Medtronic quality expectations to suppliers and partnering effectively with them to develop quality systems, processes and controls to fulfil these expectations;

+ Engaging with suppliers to execute process qualification plans and reports to assure supply of components and materials;

+ Representing the organization as the primary supplier liaison on component quality issues;

+ Participation and leading supplier quality system audits, ensuring timely and appropriate action is taken;

+ Assessment of supplier processes for optimum output, process stability and controls, identifying and implementing strategies for continual quality improvement and control;

+ Development and certification of suppliers to achieve Dock to Stock status for supplied components;

+ Monitoring, analyzing and identifying trends from supplier quality and performance data;

+ Review and disposition of supplier change requests, coordinating activities with suppliers and with internal cross-functional support teams to develop and implement appropriate strategies to qualify and support the change;

+ Review and evaluate changes to Medtronic specifications for purchased components and materials, ensuring changes are consistent with quality objectives;

+ Functioning effectively as part of cross functional and cross organizational teams, developing strong partnering relationships with Suppliers, Supply Chain, Design, Manufacturing and Quality groups.

+ Work on occasion in a cleanroom setting following protective procedural requirements.

+ Complete other tasks as assigned by the site QA Manager.

**Must have**

+ Bachelor degree in Quality, Science, Mechanical or Polymer Engineering.

+ 2/4 years of experience in a QA/QC department at a Medical Device, Pharmaceutical, Biotech or other regulated industry.

+ Excellent organizational, leadership, decision-making and analytical skills.

+ Well-developed inter-personal and teamwork skills to communicate and resolve product quality issues

+ Demonstrated ability to multi-task resulting in positive outcome for each task assigned or self-generated.

+ Experience with and knowledge ofISO9001 and/or ISO 13485.

+ Experience to work with ERP, statistical techniques, and other software office applications.

+ Fluent in English, knowledge of Dutch and/or German is preferred.

**Your Answer**

Is this the position you were waiting for? Then please apply directly via the apply button!

**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.

Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.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.

As a global leader in medical technology, we serve patients and partner with medical professionals in 120 countries. Below are our main regional offices; key manufacturing, service, and research and development facilities; and Bakken Education Centers for physician training.

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