Overview
On Site
Hybrid
USD 50.00 per hour
Full Time
Skills
Electrical Engineering
Biomedicine
Mechanical Engineering
Software Engineering
Electromechanics
Medical Devices
Military
Computer Hardware
Analytical Skill
Communication
Systems Engineering
Product Development
Surveillance
Human Factors And Ergonomics
Product Design
Research
SAFE
Problem Solving
Conflict Resolution
SAP BASIS
Field Service
Manufacturing
ISO 9000
Design Controls
IBM Rational DOORS
Mentorship
Management
Job Details
Date Posted: 05/02/2025
Hiring Organization: Rose International
Position Number: 482118
Job Title: Systems Engineer
Job Location: Plymouth, MN, USA, 55441
Work Model: Hybrid
Employment Type: Temporary
Estimated Duration (In months): 12
Min Hourly Rate($): 50.00
Max Hourly Rate($): 55.00
Must Have Skills/Attributes: DHF, Electro Mechanical, Firmware, FMEA, Medical device, Systems Engineering
Job Description
***Only qualified Systems Engineer candidates located near Plymouth, MN area to be considered due to the position requiring an onsite presence***
Education:
A bachelor's degree in electrical, Mechanical, Biomedical, Controls, and Systems, Software or another related technical/engineering field
Experience:
3+ years of industry work experience
Must possess sound knowledge of systems engineering and related areas such as electro-mechanical and software engineering
Qualifications:
A demonstrated track record in electromechanical system development, preferably medical devices or other highly regulated products such as military hardware
Demonstrated strong analytical and problem-solving skills
Success in working with multi-functional, global teams
Excellent interpersonal/communication/influencing skills
Essential Duties and Responsibilities
Perform the activities associated with the Systems Engineering of one or more products in different stages of the product lifecycle from new product development to post-market surveillance
Understand clinical and user needs and apply them to product realization
Capture inputs for Requirements from various sources such as Standards, User needs, Regulatory, Quality, Human factors, Manufacturing, Service, etc.
Use knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a Systems perspective
Initiate, develop, and lead feasibility by crafting design concepts and research methodologies that best meet both current and future customer / business needs for a product or process domain area
Build and maintain Design History File elements and ensure traceability to requirements
Facilitate an improved understanding of the interrelationship between Requirements, Risk and Reliability
Anticipate technical challenges and risk scenarios and then prepare, lead, and execute mitigation strategies to ensure safe and effective results
Resolve systems-related technical issues by applying problem-solving tools such as cause-and-effect diagrams, Pareto charts, etc.
Propose and drive solutions to technical problems that are ambiguous and diverse in scope
Perform impact assessments on the Requirements on an ongoing basis for any proposed design/material/process change or an observation in the field/service or manufacturing to determine the impact and need for any mitigations, then propose recommended mitigations with the rationale
Influence partners and multi-functional team members within the project
Drive consistency to FDA, ISO and IEC design control procedures, regulations and standards
Use various software tools and programs (e.g. DOORS) to complete the above responsibilities
Teach and mentor others in life cycle management methodologies
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
Hiring Organization: Rose International
Position Number: 482118
Job Title: Systems Engineer
Job Location: Plymouth, MN, USA, 55441
Work Model: Hybrid
Employment Type: Temporary
Estimated Duration (In months): 12
Min Hourly Rate($): 50.00
Max Hourly Rate($): 55.00
Must Have Skills/Attributes: DHF, Electro Mechanical, Firmware, FMEA, Medical device, Systems Engineering
Job Description
***Only qualified Systems Engineer candidates located near Plymouth, MN area to be considered due to the position requiring an onsite presence***
Education:
A bachelor's degree in electrical, Mechanical, Biomedical, Controls, and Systems, Software or another related technical/engineering field
Experience:
3+ years of industry work experience
Must possess sound knowledge of systems engineering and related areas such as electro-mechanical and software engineering
Qualifications:
A demonstrated track record in electromechanical system development, preferably medical devices or other highly regulated products such as military hardware
Demonstrated strong analytical and problem-solving skills
Success in working with multi-functional, global teams
Excellent interpersonal/communication/influencing skills
Essential Duties and Responsibilities
Perform the activities associated with the Systems Engineering of one or more products in different stages of the product lifecycle from new product development to post-market surveillance
Understand clinical and user needs and apply them to product realization
Capture inputs for Requirements from various sources such as Standards, User needs, Regulatory, Quality, Human factors, Manufacturing, Service, etc.
Use knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a Systems perspective
Initiate, develop, and lead feasibility by crafting design concepts and research methodologies that best meet both current and future customer / business needs for a product or process domain area
Build and maintain Design History File elements and ensure traceability to requirements
Facilitate an improved understanding of the interrelationship between Requirements, Risk and Reliability
Anticipate technical challenges and risk scenarios and then prepare, lead, and execute mitigation strategies to ensure safe and effective results
Resolve systems-related technical issues by applying problem-solving tools such as cause-and-effect diagrams, Pareto charts, etc.
Propose and drive solutions to technical problems that are ambiguous and diverse in scope
Perform impact assessments on the Requirements on an ongoing basis for any proposed design/material/process change or an observation in the field/service or manufacturing to determine the impact and need for any mitigations, then propose recommended mitigations with the rationale
Influence partners and multi-functional team members within the project
Drive consistency to FDA, ISO and IEC design control procedures, regulations and standards
Use various software tools and programs (e.g. DOORS) to complete the above responsibilities
Teach and mentor others in life cycle management methodologies
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
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.