1+ months

Production Quality engineer

Rockwood, TN 37854
Production Quality engineer


Yokneam, Industrial Zone, HaTsafon, Israel

Requisition #:


Post Date:

Dec 02, 2019

**Careers that Change Lives**

Were a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Join our team in Operations Quality Assurance and help shape policies that change lives.

Work with us to incentivize better patient care, and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.

Come strengthen your specialized skills and enhance your expertise. Well support you with the training, mentorship, guidance, and networks you need to advance, and empower you to work in the way thats best for you.

Together, we can confront the challenges that will change the face of healthcare. Join us for a career that changes lives.

**A Day in the Life**

as a Production Quality engineer in Ops. QA department you will:

Lead and maintain product quality plans activities throughout product life cycle, from design transfer to post market, including but not limited to: DMR, DHR, Control Plans.

Champion problem solving and root cause analysis activities in production line to eliminate recurrence of nonconformances

Serve as quality liaison for production line and ensure corporate standards, procedures and tools implementation and compliance

Serve as subject matter expert for manufacturing engineering processes such as process validation, MSA, pFMEA etc.

Lead and support sustainability and improvement projects

Monitor, communicate and seek improvement of quality KPIs

Lead and participate in internal and external audits

Communicate manufacturing quality standards and requirements within the organization, support training activities and implementation of quality culture

**Must Have:**

Electrical/Mechanical/Biomedical/Quality Engineer

Minimum 3 years of experience as quality engineer in the Medical device/aerospace/pharma industry

Knowledge in Medical device standards and Regulations (ISO13485, QSR, MDR, ANVISA etc.)

Good control in statistical techniques

Experience with 8D, Lean, 5 Whys, Pareto Analysis, Six Sigma, 8D, DFSS, dFMEA, pFEMA, PPAP, Process Validation etc.

Strong written and verbal communication skills

Strong problem-solving skills

Strong organizational skills

**Nice Have:**


6 Green/Black Belt

**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.


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. 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.
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: 2019-12-05 Expires: 2020-02-09

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Production Quality engineer

Rockwood, TN 37854

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