Principal Systems Engineer

Minnesota City, MN, US • Posted 3 days ago • Updated 5 hours ago
Contract Corp To Corp
Travel Required
On-site
Company Branding Image
Fitment

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Job Details

Skills

  • Technical Documentation
  • communication skills
  • ISO 13485
  • Data Analysis
  • Systems Engineering
  • Problem solving
  • Regulatory Compliance
  • Quality Control
  • Mentoring
  • Usability Testing
  • Performance Testing
  • Scheduling
  • Manufacturing Processes
  • Ergonomics
  • manufacturing
  • Electronics Manufacturing
  • Product Design
  • Circuit Design
  • Design Control
  • Design Development
  • Intellectual Property
  • Testing Skills
  • Coordination Skills
  • Self Motivation
  • Software Engineering
  • Blueprinting
  • Health Care
  • Assembly and Installation
  • Machinery
  • Systems Development Life Cycle
  • Medical Materials
  • Ability to Multitask
  • Programme Management
  • Computer Architecture
  • Design Specifications
  • Engineering Design Process
  • Printed Circuit Board
  • Electrical Wirings
  • FDA Regulations
  • Finite Element Methods
  • Medical Guidelines
  • Prioritisation of Requirements
  • Sub Assemblies
  • Task Management
  • Test Methods
  • Writing of Reports
  • Basic Engineering
  • Franchising Skills
  • Knowledge of Electrical Engineering
  • Research and Development

Summary

Job Title: Principal Systems Engineers

Location: Minnetonka, MN, Onsite role

Experience : 10+ Years

Looking for talented Principal Systems Engineers to join our growing team in Minnetonka, MN! Systems thinker who loves solving complex engineering challenges that actually save lives...

POSITION SUMMARY:

This position will contribute to the company success through the design and development of capital equipment and devices. This position will report to the Senior Director, Research and Development in the Franchise. The individual will work on capital equipment projects to design, build, and test next generation capital equipment that is used by cardiac surgeons and electrophysiologists. This position contributes in a collaborative way with management, project teams, production associates, external vendors and other work groups to achieve the company's goals of producing market-lead products through positive patient outcomes. The Principal Systems Engineer may work independently on projects with broad scope or be a team member on PD project.

ESSENTIAL FUNCTIONS OF THE POSITION:

  • Define and lead system development tasks to include design, integration, and formal testing of capital equipment and devices
  • Develop and complete actions in system specifications, technical and logistical requirements, and other disciplines
  • Identify and develop a rapport with key customers surgeons, nurses, and other clinicians
  • Develop in-depth understanding of clinical procedures and techniques applicable to AtriCure products
  • Create and maintain programmatic and technical documentation to ensure efficient planning and execution
  • Aligns and coordinates resources, priorities, work plans, and activities among outside suppliers and the AtriCure Product Development group
  • Determines work procedures, prepares work schedules, and expedites workflow
  • Design, develop and test all aspects of electrical components, equipment and machinery
  • Communicate with and direct external suppliers of components, subassemblies and finished assemblies.
  • Generate and document intellectual property
  • Develop and perform stress and performance tests on a variety of electrical/electronic system hardware including circuit boards, processors and wiring
  • Perform a variety of complex engineering design and development tasks, to include design, testing and analysis, verification, and validation
  • Develop and validate test methods
  • Review and authorize engineering design changes
  • Develop component and product technical specifications including the integration and consideration of applicable standards and regulations
  • Mentor junior engineers

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION:

  • Regular and predictable work performance
  • Ability to work under fast-paced conditions
  • Ability to make decisions and use good judgement
  • Ability to prioritize various duties and multitask as required
  • Ability to successfully work with others
  • Additional duties as assigned

BASIC QUALIFICATIONS:

  • BS in Engineering
  • 15+ years of experience in systems engineering or equivalent field
  • Demonstrated skills in System engineering
  • Experience in hardware/software development methodologies and structured approaches to system development
  • Must be proficient acting in and leading integrated process teams, as well as coordinating and communicating customer requirements
  • Demonstrated understanding of circuits and circuit design
  • Understanding of program management tools and expectations of medical device design and manufacturing controls
  • Experience working with customers and translating the "Voice of the Customer" into technical specifications
  • Demonstrated understanding of protocol/report writing
  • Experience with data analysis, problem-solving, and troubleshooting
  • Knowledge of Design Controls and experience with FDA QSR 21 CFR Part 820 and ISO 13485
  • Ability to read technical specifications, blueprints, and drawings
  • Capable of prioritizing tasks and provide a timely schedule of completion
  • Capable of sub-assembly level analysis (not limited to circuit, tolerance or finite element analysis)
  • Demonstrated proficiencies of communicating best practices
  • Experience with International Usability Standards and the practical application of Usability Engineering
  • Ability to travel 25%

PREFERRED QUALIFICATIONS:

  • MS degree in Systems Engineering or Electrical Engineering
  • Excellent demonstrated skills in System engineering
  • Vast Experience in hardware/software development methodologies and structured approaches to system development
  • Demonstrated proficiency in leading integrated process teams, as well as coordinating and communicating customer requirements
  • Excellent written and oral communication skills
  • Excellent understanding of industry regulations as it pertains to medical devices
  • Excellent understanding of external standards, design controls, quality controls, manufacturing methods
  • Proven track record of generating and documenting intellectual property
  • Experience with Human Factors for medical devices/equipment
  • Expertise with International Usability Standards and the practical application of Usability Engineering

OTHER REQUIREMENTS:

  • Ability to regularly walk, sit, or stand as needed
  • Ability to occasionally bend and push/pull as needed
  • Ability to regularly lift up to 25 pounds, occasionally lift over 25 pounds
  • Ability to pass pre-employment drug screen and background check

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91122967
  • Position Id: 2026-4281
  • Posted 3 days ago

Company Info

About ADDSOURCE

AddSource is a premier staffing and workforce solutions partner headquartered  in  Delaware,  USA,  with  operations  in  Alberta,  Canada  under  the  brand  name AddSource.

We  specialize  in  connecting  top-tier  talent  with  leading organizations across diverse industry sectors.

With  a  strong  commitment  to  excellence,  our  mission  is  to deliver innovative, customized staffing solutions that empower clients  to  achieve  their  goals  while  helping  candidates advance their careers.

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