Medtronic

Quality Technician V - MCS

Medtronic$76K — $114K *
Miami, FL 33186In-Person
Healthcare
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • High School diploma with 15 years of technical experience
  • Exposure to quality engineering practices
  • Effective communicator with customers and vendors
  • Experience with medical device regulations
  • Familiarity or experience with Ventricular Assist Devices (VADs)
  • Six Sigma Yellow Belt certification
  • Certification in root cause analysis methodology

Responsibilities

  • Collaborate with engineering and manufacturing to uphold quality standards
  • Ensure corrective measures meet reliability standards and comply with documentation requirements
  • Specialize in various quality assurance areas like design, production control, and reliability
  • Conduct comprehensive reviews of HVAD log files to ascertain malfunction causes
  • Analyze HVAD system test results to identify probable root causes of reported events
  • Assess interactions between reported malfunctions and HVAD system components
  • Create detailed HVAD investigation reports for regulatory compliance and findings
  • Lead projects to enhance analysis processes and reduce waste

Benefits

  • Health, dental, and vision insurance
  • Health Savings Account and Healthcare Flexible Spending Account
  • Tuition assistance and reimbursement
  • 401(k) plan with employer contributions
  • Paid time off and holidays
  • Employee Stock Purchase Plan
  • Global well-being program (Simple Steps)
Full Job Description
We anticipate the application window for this opening will close on - 8 Jun 2026

A Day in the Life
Quality Technician V

Medtronic Mechanical Circulatory Support (MCS) is seeking a Quality Technician V to join the MCS Complaint Investigation team to perform complex failure analysis of devices/components returned with alleged malfunctions, collaborate with engineering, product development, complaint management, supplier quality and manufacturing functions to ensure returned product investigations fully address reported events and assist in developing and implementing methods and procedures to assist in product analysis investigations improvement. Perform a variety of qualitative tests and validation of new tools, designed to improve the analysis process performance and accuracy.

This position is in Miami Lakes, FL. within the Mechanical Circulatory Support (MCS) operating unit. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We are working on-site 4 days per week as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects.

A Day in the Life

In general, the following responsibilities apply for the Quality Technician V role. This includes, but is not limited to the following:

  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • 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.
  • Completes comprehensive review of HVAD log files to determine correlation between the reported event and electro-mechanic components.
  • Reviews HVAD system testing results including but not limited to: profilometer measurements, front/back impeller pre-loads, axial gap measurements, in-vitro wet-test functional parameters, and stators conductivity results to determine a most probable root cause associated with a reported event.
  • Determines potential interaction between reported event and all HVAD system components controller, batteries, pump, monitor, AC adapter, battery charger, and surgical tools.
  • Generates comprehensive HVAD product investigation reports to support findings, root cause, regulatory requirements and obtains the necessary release approvals.
  • Creates and develops engineering projects for improvements of analysis/investigation process to eliminate process waste and reduce rework rates.
  • Participates and/or conducts validation or qualifications tests of new or existing failure analysis equipment in accordance with internal procedures.


Qualifications

Must Have: Minimum Requirements

TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME

  • High School diploma and 15 years of experience technical experience


Nice to Have
  • Exposure to quality engineering best practices and timely resolution of nonconforming product issues.
  • Demonstrated track record of communicating effectively with internal and external employees, customers, and vendors regarding ongoing operations.
  • Uses information exchange, influence, and active persuasion without direct exercise of command to gain cooperation of supporting functions.
  • Familiarity with medical device regulations and good manufacturing practices
  • Experience with VADs
  • Six sigma yellow belt certification.
  • Root cause analysis methodology certification.


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)

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. a7 214.2(h)(4)(iii)(A) is required.

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.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Join us in our mission to alleviate pain, restore health, and extend life-where your unique background and perspective are valued.
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):$76,000.00 - $114,000.00

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

Medtronic plc is an Irish-domiciled multinational medical device company that develops and manufactures medical device technologies and therapies to treat chronic diseases worldwide. Medtronic was founded in 1949 in Minneapolis, Minnesota, as a medical equipment repair shop. Today, the company operates in more than 160 countries and employs over 90,000 people. Medtronic's primary products include implantable pacemakers and defibrillators, insulin pumps, spinal and neurostimulation devices, surgical tools, and patient monitoring systems. The company is committed to improving patient outcomes and expanding access to healthcare through innovative medical technologies.
Learn more about Medtronic
Size
95,000 employees
Market Cap
$102.7 billion
Industry
Net Income
$2.8 billion
Founded
1949
5 Year Trend
+1.3%
Revenue
$27.9 billion
NASDAQ

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