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Senior Quality Engineer
Medtronic Jacksonville, FL
$82k-97k (estimate)
Full Time | Medical Technology 9 Months Ago
Save

Medtronic is Hiring a Senior Quality Engineer Near Jacksonville, FL

Careers that Change Lives

Our space, the medical device and healthcare industry, is rapidly changing. It always has been that way. With remote monitoring, wearables, robotics, AR/VR, telemedicine, and much more, agility and responsiveness are key to our success. Experience what it’s like to work at a company with an exciting product pipeline full of patented inventions driving innovation in the healthcare space.

The Ear, Nose, and Throat Operating Unit is a global leader and trusted partner for innovative ENT solutions that improve patient access, outcomes, and customer satisfaction. We partner with the ENT community to understand the needs of customers and patients, delivering solutions that improve lives as we embody a culture of accountability and trust.

Over the past 20 years, we have become the global market leader in three key segments – image-guided surgery, intraoperative nerve monitoring, and powered surgical instruments. We continue to launch valuable ENT solutions in these areas as well as tissue health and balloon sinus dilation.

A Day in the Life

Responsibilities 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.
  • Reviews master test plans that encompass Design Verification/Validation, and Test Method Validation activities.
  • Provide guidance to Engineering staff and other personnel and ensures that Design Control requirements are being met in an effective manner, including Design Input/Output, Design Verification/Validation, Risk Management, Test Method Validation and Component Qualification.
  • 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 related projects, product, or process quality.
Must Have: Minimum Requirements
 
  • Bachelors degree required
  • Minimum of 4 years of Quality Engineering experience, or advanced degree with a minimum of 2 years relevant experience
Nice to Have
  • Strong knowledge of design development and Design History File in accordance with 13485/FDA 21 CFR 820 including Design Input/Output, Design Verification/Validation, Risk Management, Test Method Validation and Component Qualification.
  • Must be self-motivated to complete assigned tasks on time.
  • Must be able to multitask on number of assigned projects/assignments

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)

A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Learn more about our benefits here. 

This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) here.

The provided base salary range is used nationally (except in certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Medical Technology

SALARY

$82k-97k (estimate)

POST DATE

08/24/2023

EXPIRATION DATE

06/07/2024

WEBSITE

medtronic.com

HEADQUARTERS

WASHINGTON, DC

SIZE

>50,000

FOUNDED

1949

TYPE

Public

CEO

PETER B SLONE

REVENUE

$3B - $5B

INDUSTRY

Medical Technology

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Medtronic is a medical technology and services firm that manufactures devices and therapies to treat for chronic diseases.

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