Job Details

ID #51892350
Estado Minnesota
Ciudad Fridley
Full-time
Salario USD TBD TBD
Fuente Medtronic
Showed 2024-06-12
Fecha 2024-06-13
Fecha tope 2024-08-12
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Associate Quality Engineer - Neuromodulation - Rice Creek, MN (Onsite)

Minnesota, Fridley 00000 Fridley USA
Aplica ya

Careers That Change LivesA career at Medtronic is like no other. We’re purposeful. We’re committed. And we’re driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide.In this exciting role as a Associate Quality Engineer you will have responsibility for ensuring our products exceed the safety and reliability requirements and expectations of patients, clinicians, regulators, and the business.This position provides quality engineering on new product development teams for R&D. The candidate will be a key player in cross-functional teams and serve as a representative for reliability, safety and quality functions.As part of R&D project teams, the Quality Engineer will support to define, contribute, and execute the overall reliability strategy on programs. This position will work with multidisciplinary teams and support Design for Reliability (DfR), provide guidance to technical issues, engage in design, and risk reviews, and contribute to development activities.Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. It’s no accident – we work hard to cultivate a workforce that reflects our patients and partners. We believe it’s the only way to drive healthcare forward and remain a global leader in medical technology and solutions.To learn more about Inclusion & Diversity at Medtronic Click Here (https://www.medtronic.com/us-en/about/careers/diversity-inclusion.html)Location : Rice Creek East, MNAbility to travel up to : Less than 2%, as needed (Domestic and/or International)A Day in the LifeResponsibilities may include the following and other duties may be assigned.

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 .

Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A), 0 years of experience required.

Requires broad theoretical job knowledge typically obtained through advanced education.

Nice to Have ( Preferred Qualifications )

Advanced degree in Engineering or Science.

Understanding of reliability engineering principles.

Experience in the application of statistics.

Experience in a highly regulated industry, preferably implantable medical devices.

Experience with 21 CFR Part 820 (Quality System Regulation), ISO 13485, etc.

Experience in the application of Risk Management (ISO 14971) and hazard analysis and risk analysis techniques (e.g., PHA, HA, FTA, DFMEA).

Ability to independently lead investigations to identify system/product failures, hazards, hazardous situations, and harms.

Exposure to or experience working in or with Design, Quality, Regulatory, Clinical and/or Manufacturing.

Knowledge of Design for Reliability (DfR), Design for Reliability and Manufacturability (DRM), Design for Six Sigma (DFSS), Design for Lean Sigma (DFLS), and/or robust design practices.

About MedtronicTogether, 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 RequirementsThe 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).Min Salary62400Max Salary93600It 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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