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R&D Engineer II

Medtronic
Fort Worth, United Statesfull_timeVerifiedPosted 22 Oct 2025
💰 $124,800/yr

About the role

We anticipate the application window for this opening will close on - 30 Oct 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

This position supports the design and development of new products and product improvements. Responsibilities will also include developing, implementing, and improving Quality Management System (QMS) procedures. Also supports project planning and project management. Provides engineering and technical support to other functional areas of the company as required.

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’re working a minimum of 4 days a week, onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. 

Travel requirement: Less than 10%

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

  • Provides engineering support for new product design and development, existing product modifications, process design, and performance evaluation.
  • Use computer-assisted engineering and design software and equipment to perform engineering and design tasks.
  • Develops and tests prototypes based on design specifications, defines processes to properly manufacture and assemble the product, and optimizes the manufacturing process.
  • Develops product and process verification and validation, test protocols, and reports in compliance with design control requirements. 
  • Analyzes test data and reports to determine if designs meet functional and performance requirements.
  • Support updates and improvements to QMS procedures.
  • Evaluate the impact of external standard changes on products and their DHFs.
  • Leverage knowledge of Risk Management, Regulations, and Procedures to ensure continued product compliance.
  • Provides test reports, drawings, and other requirements to the RA necessary for preparing regulatory notifications and submissions 510(k)s and PMAs for domestic and international approvals as required.
  • Determines realistic start and finish dates for action items imperative to project completion on the project schedule and submits to the project team leader.  Updates project schedule as required.
  • Identify areas for improvement in manufacturing, lab tooling, and technical processes across all project phases and recommend changes to the appropriate management.  Provides production line support when required.
  • Provides technical training for appropriate Lab and Production personnel as appropriate.
  • Reviews appropriate technical literature for the necessary background on specific assignments.
  • All activities must be performed in compliance with the Quality System.
  • Performs duties in compliance with environmental, health, and safety-related site rules, policies, or government regulations.

Must Have: Minimum Requirements

  • Bachelor’s degree in mechanical engineering
  • 2+ years of related experience with a bachelor’s degree.

Nice to Have

  • Advanced degree.
  • Familiar with working in an ISO 13485 and FDA-regulated environment
  • Experienced in QMS procedures, regulations, and standards.
  • Experience with Risk Management
  • Experience with material selection.
  • Understanding and application of statistical methods
  • Experience with data acquisition and statistical analysis software
  • Experience with projects from concept to completion. Experience with the design of mechanical and/or electromechanical devices.
  • Experience developing test methods, test execution, and report writing.
  • Experience with computer software: MS Office, ProEngineer, etc.
  • Basic understanding of statistical methods

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 in

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Company

Medtronic

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