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Quality Engineer I

We anticipate the application window for this opening will close on - 8 Apr 2025


 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

We anticipate the application window for this opening will close on - 8 April 2025.

Join our dynamic team at Medtronic's Fort Worth manufacturing site as a Quality Engineer I, where you'll play a crucial role in ensuring the highest standards of product quality and compliance. As a Quality Engineer, you will be at the forefront of driving continuous improvement initiatives, collaborating with cross-functional teams to enhance processes, and ensuring that our products meet rigorous industry standards. This position offers an exciting opportunity to grow your career in a fast-paced environment, contributing to Medtronic's mission of improving lives through innovative medical solutions. If you're passionate about quality, detail-oriented, and eager to make a difference, we invite you to explore this rewarding opportunity.

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.

  • 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.

Minimum Requirements: 

  • Bachelor's degree with 0 years of relevant experience.

Nice to Have

  • Knowledge of Gage R&R activities, process validation, process verification and process monitoring.

  • Experience with Advantive/InfinityQS Proficient SPC a plus.

  • Experience and or knowledge of programming inspection equipment.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

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.

Benefits & Compensation
 

Medtronic offers a competitive Salary and flexible Benefits Package
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.
 

Salary ranges for U.S (excl. PR) locations (USD):$62,400.00 - $93,600.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

 

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

 

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

 

Further details are available at the link below:

Medtronic benefits and compensation plans

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here.

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.

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

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Average salary estimate

$78000 / YEARLY (est.)
min
max
$62400K
$93600K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Quality Engineer I, Medtronic

Join Medtronic as a Quality Engineer I in Fort Worth, Texas, and step into a role that combines your passion for quality with a commitment to innovation in healthcare. At Medtronic, you’ll be part of a dynamic team where your efforts will directly impact the quality of medical solutions that change lives. As a Quality Engineer, your day-to-day responsibilities will include developing, modifying, and maintaining quality standards crucial for product processing, ensuring compliance with industry regulations. You'll collaborate with talented engineers and manufacturing personnel to forge strong quality processes that safeguard our commitment to excellence. Being at the forefront of quality control means you’ll devise methods of testing and evaluating products, ensuring that every item meets the highest standards before reaching patients. And, with a variety of exciting projects, you’ll also get to specialize in key areas such as design and research. Moreover, Medtronic fosters a culture of continuous improvement, so you’ll have the opportunity to drive initiatives while honing your skills and advancing your career in a supportive environment. If attention to detail and a desire to make a real impact define your work ethic, this position could be your gateway to a rewarding career. Don’t miss out on this chance to be part of an organization dedicated to alleviating pain and extending lives through pioneering technology. Explore this exciting opportunity today and unlock your potential with Medtronic!

Frequently Asked Questions (FAQs) for Quality Engineer I Role at Medtronic
What are the key responsibilities of a Quality Engineer I at Medtronic?

As a Quality Engineer I at Medtronic, your primary responsibilities will include developing and upholding quality standards and protocols for both partially finished and finished products, collaborating with engineering and manufacturing teams, and implementing methods for inspecting and testing products. This role emphasizes continuous improvement, ensuring that all products meet rigorous standards and specifications to enhance quality assurance processes.

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What are the qualifications needed to apply for the Quality Engineer I position at Medtronic?

To qualify for the Quality Engineer I position at Medtronic, a bachelor’s degree is required with zero years of relevant work experience. However, familiarity with Gage R&R activities and process validation is considered an advantage. Candidates with experience or knowledge in programming inspection equipment may also stand out during the application process.

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How does Medtronic support the professional growth of its Quality Engineer I employees?

At Medtronic, employees in the Quality Engineer I position are encouraged to pursue continuous learning and professional development. The company offers various training programs, mentorship opportunities, and the chance to be involved in innovative projects that drive personal growth and career advancement. Collaborating with cross-functional teams allows you to enhance your skills while contributing to meaningful improvements in healthcare.

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What benefits does Medtronic provide for Quality Engineer I employees?

Medtronic offers a competitive salary and a comprehensive benefits package for Quality Engineer I employees, including health, dental, and vision insurance, 401(k) plans with employer contributions, tuition assistance, and generous paid time off. Additionally, employees can participate in incentive plans and take advantage of well-being programs. This commitment to employee welfare reflects Medtronic's core values.

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What does a typical day look like for a Quality Engineer I at Medtronic?

A typical day for a Quality Engineer I at Medtronic is filled with engaging projects and collaborative meetings. You will actively participate in quality inspections, work on developing new protocols, and communicate with different departments to address quality issues. The environment is fast-paced and focused on continuous improvement, making your contributions essential to ensuring the success of our innovative medical solutions.

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Common Interview Questions for Quality Engineer I
Can you describe your experience with quality assurance in engineering?

When answering this question, focus on specific projects and experiences where you successfully implemented quality assurance processes. Detail any methodologies you used and emphasize how your contributions improved product quality, demonstrating your understanding of quality standards.

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How do you ensure compliance with industry standards?

Discuss your familiarity with relevant industry standards and regulatory requirements. Explain how you would stay updated with changes in compliance regulations and outline your process for verifying that quality protocols are always met.

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What techniques do you use for statistical analysis in quality control?

Highlight specific statistical tools or software you have used in the past for quality control, such as Six Sigma or Statistical Process Control (SPC). Explain how you would apply these techniques to assess quality data and make informed decisions.

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Describe a challenge you faced in quality engineering and how you overcame it.

Use the STAR method (Situation, Task, Action, Result) to present a clear narrative of a challenge. Detail the issue, your role in addressing it, and the outcome, ensuring it showcases your problem-solving skills and resilience in maintaining quality standards.

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How do you prioritize tasks when working on multiple projects?

Emphasize your organizational skills and methods for prioritization. You could describe a system you use, such as task management software or a prioritization matrix, showcasing your ability to manage workloads effectively.

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What role does teamwork play in quality engineering?

Discuss the importance of collaboration in quality engineering. Highlight experiences where teamwork led to successful outcomes and share how you would facilitate communication and cooperation among cross-functional teams.

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How would you approach developing new quality standards?

Outline your strategic approach to developing new quality standards, incorporating research, collaboration with stakeholders, and testing. Emphasize your desire for continuous improvement and ensuring that new standards align with overall organizational goals.

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What is your understanding of Gage R&R?

Demonstrate your knowledge of Gage R&R by explaining the concept and its significance in quality engineering. Share any experiences you have with measurement systems analysis and how it impacts product quality.

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How would you handle a product that fails to meet quality standards?

Outline a systematic approach to investigating the failure, documenting findings, and devising corrective actions. Emphasize the importance of thorough analysis, and collaboration with engineering teams to implement solutions.

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Why do you want to work at Medtronic as a Quality Engineer I?

Express your alignment with Medtronic’s mission to improve lives through innovation. Share your enthusiasm for contributing to projects that have a direct impact on patient care, and highlight Medtronic's commitment to employee growth, which resonates with your career goals.

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Mission Written in 1960, our Mission dictates that our first and foremost priority is to contribute to human welfare. Over a half-century later, the Mission continues to serve as our ethical framework and inspirational goal for our employees aroun...

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DATE POSTED
April 3, 2025

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