Research & Development Engineer I at Medtronic
Memphis, TN 38116, USA -
Full Time


Start Date

Immediate

Expiry Date

01 Dec, 25

Salary

69600.0

Posted On

01 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Optimization, Design, Protocol, Components, Completion, Product Design, Disabilities, Defining Requirements, Iso, Design Specifications, Pmas, Deliverables, System Architecture, Ptc Creo, Iec, Preparation, Gage R&R, Qsr, Engineering Support, Process Validation

Industry

Other Industry

Description

We anticipate the application window for this opening will close on - 2 Sep 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.

REQUIRED KNOWLEDGE AND EXPERIENCE:

  • Requires a Baccalaureate degree

Nice to Have (This is your Wish List) .

  • Provide engineering support for new product design and development, including existing product modifications, process design, development, optimization, and performance evaluation.
  • Coordinate projects/stages/processes within Product Development.
  • Contributes towards planning and completion of deliverables through building relationships and consensus.
  • Defining requirements and system architecture for new product development for spinal instruments and implants.
  • Responsible for the design of components, sub-assembly products using PTC Creo.
  • Develop and test prototypes from design specifications, define processes to properly make and assemble the product, and optimize the process.
  • Coordinate various programs, which include FMEA (Failure Mode and Effects Analysis) and Risk Assessments.
  • Coordinate Process Validation, DOE (Design of Experiments), Gage R&R (Gage Repeatability & Reproducibility), and GD&T (Geometric Dimensioning and Tolerancing).
  • Utilize various failure investigation techniques, statistical quality control, protocol & report preparation, and non-conforming product controls.
  • Navigate the complexities of government and industry regulations to include QSR (Quality Systems Regulation) 21 CFR 820, ISO 13485, ISO 9001, IEC 60601, and ISO 14971 (for product development in the medical device industry).
  • Develop protocols for design validation and verification.
  • Provide technical support for regulatory notifications and submissions using 510(k)s and PMAs for domestic and international approvals.

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.

Responsibilities
  • Designs, develops, analyzes, troubleshoots, and provides technical skills during research and/or product development.
  • Designs studies to investigate specific life science questions within the field of expertise.
  • May be involved in product research and development and/or clinical trials.
  • Translates research discoveries into usable and marketable products
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