PP
Test Engineer - Medical Device (Junior Level)
Accepting applicationsPlanet Pharma · Minneapolis, MN
Contract Associate
Posted
11 Jun
Category
Verification
Experience
Associate
Country
United States
Job ID: 628563
Our client, a leading Medical Device company, is seeking a junior level Test Engineer for their growing team in Minneapolis. This is perfect for an early-career candidate who is willing to learn and be adaptable to take on various tasks. See below for other details!
Skills Needed:
Adaptability
Ability to Quickly Learn New Concepts
Familiarity with Medical Device Design Verification (preferred)
Main Responsibilities / Day-to-Day Activities
Design Verification Execution: Test Method Development; Test Method Validation; Test Method Execution
Managing Technicians during Test Method Execution
Writing Design Verification Protocols
Analyzing Test Data and Writing Design Verification Reports
Key Responsibilities:
Design and Development: Plan, design, develop, and verify mechanical and electromechanical systems,
Project Management: Support projects through all stages, from R&D to manufacturing, ensuring they meet product requirements, technical specifications, timelines, and budget constraints.
Innovation and Improvement: Recommend and implement options or approaches to enhance safety, performance, efficiency, and cost-effectiveness of systems, processes, and facilities.
Collaboration: Work closely with cross-functional teams, including electrical and systems engineers, to deliver integrated solutions.
Problem Solving: Analyze engineering problems, providing in-depth analysis and innovative solutions to improve processes and products.
Prototyping and Testing: Oversee the creation of prototypes and conduct testing to characterize, refine, and verify designs. This role will also be responsible for design characterization and design verification protocols, analysis and reports. This role could also include aspects of test equipment qualification and test method validation.
Documentation and Compliance: Prepare detailed engineering documentation and ensure designs comply with industry standards, regulatory requirements, and department best practices.
Communication and Influence: Communicate effectively with senior internal and external stakeholders
Requirements:
Bachelor's Degree within an Engineering realm
1-2 years of experience within medical devices (internship time is inclusive)
Show more Show less
Our client, a leading Medical Device company, is seeking a junior level Test Engineer for their growing team in Minneapolis. This is perfect for an early-career candidate who is willing to learn and be adaptable to take on various tasks. See below for other details!
Skills Needed:
Adaptability
Ability to Quickly Learn New Concepts
Familiarity with Medical Device Design Verification (preferred)
Main Responsibilities / Day-to-Day Activities
Design Verification Execution: Test Method Development; Test Method Validation; Test Method Execution
Managing Technicians during Test Method Execution
Writing Design Verification Protocols
Analyzing Test Data and Writing Design Verification Reports
Key Responsibilities:
Design and Development: Plan, design, develop, and verify mechanical and electromechanical systems,
Project Management: Support projects through all stages, from R&D to manufacturing, ensuring they meet product requirements, technical specifications, timelines, and budget constraints.
Innovation and Improvement: Recommend and implement options or approaches to enhance safety, performance, efficiency, and cost-effectiveness of systems, processes, and facilities.
Collaboration: Work closely with cross-functional teams, including electrical and systems engineers, to deliver integrated solutions.
Problem Solving: Analyze engineering problems, providing in-depth analysis and innovative solutions to improve processes and products.
Prototyping and Testing: Oversee the creation of prototypes and conduct testing to characterize, refine, and verify designs. This role will also be responsible for design characterization and design verification protocols, analysis and reports. This role could also include aspects of test equipment qualification and test method validation.
Documentation and Compliance: Prepare detailed engineering documentation and ensure designs comply with industry standards, regulatory requirements, and department best practices.
Communication and Influence: Communicate effectively with senior internal and external stakeholders
Requirements:
Bachelor's Degree within an Engineering realm
1-2 years of experience within medical devices (internship time is inclusive)
Show more Show less
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