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1+ months

Quality Engineer II

Medtronic
Littleton, MA 01460
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Quality Engineer II

Location:

Littleton, Massachusetts, United States

Requisition #:

21000RN3

Post Date:

Oct 19, 2021


**Careers That Change Lives**


A career at Medtronic is like no other. Were purposeful. Were committed. And were driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide.


In this exciting role as a **Quality Engineer** **II** you will have responsibility for developing and assessing the quality programs and systems to applicable standards. You will ensure the timely, accurate and independent evaluation of product performance and compliance to safety and regulatory requirements prior to market release. Provide support for new product development, evaluate product field performance and reliability, recommend corrective action, and plan for continuous improvement.


Do meaningful work, make a difference, and improve lives starting with your own.


Our efforts will have lasting impact on countless individuals and families it is an opportunity we value and take pride in.


**A Day in the Life**


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


+ Contributes to design assurance activities in support of development for electromechanical systems that utilize microcontroller technology, customized/off the shelf PCBs and software applications

+ Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.

+ Collaborates with engineering and manufacturing functions to ensure quality standards are in place.

+ Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

+ Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.

+ Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.

+ May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.


**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 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**


+ Experience in the medical device industry with an emphasis on capital equipment

+ Working knowledge of FDA Quality Systems Regulations, Medical Device Directive, ISO 13485, ISO 14971

+ Experience applying statistical methodology

+ Experience implementing process improvements

+ Experience presenting technical data to groups within and outside the organization

+ Strong analytical skills

+ Excellent communication skills

+ Ability to work effectively within team and across functions


**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.

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Posted: 2022-03-25 Expires: 2022-05-27
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Quality Engineer II

Medtronic
Littleton, MA 01460

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