Overview
On Site
USD 55.00 per hour
Full Time
Skills
Recruiting
Health Care
Biomedical Engineering
Schematics
Oscilloscope
Root Cause Analysis
ISO 9000
Automated Testing
Python
LabVIEW
Risk Management
Design Controls
Verification And Validation
Vantive
Product Requirements
Soft Skills
Documentation
Attention To Detail
Cross-functional Team
Conflict Resolution
Problem Solving
Test Methods
Supervision
Test Cases
Functional Testing
Mechanical Engineering
Electrical Engineering
Quality Assurance
Computer Hardware
Electromechanics
Laboratory Equipment
Management
Inventory
Reporting
Application Lifecycle Management
Collaboration
Research and Development
Manufacturing
Testing
Regulatory Compliance
Medical Devices
ISO 13485
Job Details
Date Posted: 07/01/2025
Hiring Organization: Rose International
Position Number: 484935
Industry: Healthcare
Job Title: Test Engineer
Job Location: Plymouth, MN, USA, 55441
Work Model: Onsite
Shift: 8 to 5
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 10
Min Hourly Rate($): 55.00
Max Hourly Rate($): 57.00
Must Have Skills/Attributes: LabView, Python, Validation
Experience Desired: 1+ years of experience in electromechanical verification & validation (V&V) (3 yrs); Ability to read and analyze electrical schematics & mechanical drawings. (3 yrs)
Required Minimum Education: Bachelor's Degree
Job Description
Required Education:
Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or a related field.
Required Technical Skills:
1+ years of experience in electromechanical verification & validation (V&V) testing (medical devices preferred).
Ability to read and analyze electrical schematics & mechanical drawings.
Hands-on experience with lab equipment:
oElectrical: Oscilloscopes, DMMs, power supplies.
oMechanical: Force/pressure gauges, calipers, thermometers, flow meters.
Familiarity with root cause analysis (RCA) and troubleshooting methodologies.
Understanding of medical device compliance standards (e.g., IEC 60601, ISO 14971, FDA regulations) is a plus.
Preferred Qualifications:
Experience with test automation tools (Python, LabVIEW, etc.).
Knowledge of risk management and design controls in a regulated industry.
As a Verification and Validation (V&V) Engineer at Vantive Acute Therapies, you will be responsible for ensuring the safety, reliability, and compliance of electromechanical medical device components and systems. You will work within a cross-functional team to develop, execute, and document test methods that validate product requirements from prototype to final production.
Required Soft Skills:
Strong documentation skills with attention to detail.
Ability to work in a fast-paced, cross-functional team environment.
Self-motivated with a hands-on, problem-solving approach.
Key Responsibilities:
Develop and execute verification test methods, protocols, and reports under supervision.
Design test cases, including methodology, test setups, equipment, and acceptance criteria.
Perform functional testing of mechanical assemblies, electrical circuits, and integrated systems.
Support pre-compliance testing, design changes, and prototype evaluations for hardware teams.
Conduct feasibility and characterization testing to assess design risks.
Execute hands-on testing in internal and third-party labs, documenting defects and failures.
Troubleshoot and perform fault isolation on electromechanical systems.
Maintain lab equipment and manage inventory.
Analyze test data against acceptance criteria and report results in ALM (Application Lifecycle Management).
Collaborate with R&D, Quality, and Manufacturing teams to refine requirements and improve testing.
Ensure compliance with medical device regulations (e.g., IEC 60601, ISO 13485).
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: 484935
Industry: Healthcare
Job Title: Test Engineer
Job Location: Plymouth, MN, USA, 55441
Work Model: Onsite
Shift: 8 to 5
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 10
Min Hourly Rate($): 55.00
Max Hourly Rate($): 57.00
Must Have Skills/Attributes: LabView, Python, Validation
Experience Desired: 1+ years of experience in electromechanical verification & validation (V&V) (3 yrs); Ability to read and analyze electrical schematics & mechanical drawings. (3 yrs)
Required Minimum Education: Bachelor's Degree
Job Description
Required Education:
Bachelor's degree in Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or a related field.
Required Technical Skills:
1+ years of experience in electromechanical verification & validation (V&V) testing (medical devices preferred).
Ability to read and analyze electrical schematics & mechanical drawings.
Hands-on experience with lab equipment:
oElectrical: Oscilloscopes, DMMs, power supplies.
oMechanical: Force/pressure gauges, calipers, thermometers, flow meters.
Familiarity with root cause analysis (RCA) and troubleshooting methodologies.
Understanding of medical device compliance standards (e.g., IEC 60601, ISO 14971, FDA regulations) is a plus.
Preferred Qualifications:
Experience with test automation tools (Python, LabVIEW, etc.).
Knowledge of risk management and design controls in a regulated industry.
As a Verification and Validation (V&V) Engineer at Vantive Acute Therapies, you will be responsible for ensuring the safety, reliability, and compliance of electromechanical medical device components and systems. You will work within a cross-functional team to develop, execute, and document test methods that validate product requirements from prototype to final production.
Required Soft Skills:
Strong documentation skills with attention to detail.
Ability to work in a fast-paced, cross-functional team environment.
Self-motivated with a hands-on, problem-solving approach.
Key Responsibilities:
Develop and execute verification test methods, protocols, and reports under supervision.
Design test cases, including methodology, test setups, equipment, and acceptance criteria.
Perform functional testing of mechanical assemblies, electrical circuits, and integrated systems.
Support pre-compliance testing, design changes, and prototype evaluations for hardware teams.
Conduct feasibility and characterization testing to assess design risks.
Execute hands-on testing in internal and third-party labs, documenting defects and failures.
Troubleshoot and perform fault isolation on electromechanical systems.
Maintain lab equipment and manage inventory.
Analyze test data against acceptance criteria and report results in ALM (Application Lifecycle Management).
Collaborate with R&D, Quality, and Manufacturing teams to refine requirements and improve testing.
Ensure compliance with medical device regulations (e.g., IEC 60601, ISO 13485).
- **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.