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Work Study Biomedical Engineering Student Jobs in Minnesota

Engineering Intern - Summer 2027

Fridley, MN · On-site

$17.25 - $22.50/hr

Our 95,000 employees work across more than 150 countries to put patients first - developing ... Engineering Intern Opportunities for Students Interns may support one or more engineering areas ...

After completing initial training, the student will be assigned an Engineer to work with. * Assist engineer in planning and implementing projects to improve production efficiency. * Assist others ...

Showing results 21-40

Work Study Biomedical Engineering Student information

What is the difference between Work Study Biomedical Engineering Student vs Biomedical Equipment Technician?

AspectWork Study Biomedical Engineering StudentBiomedical Equipment Technician
CredentialsTypically enrolled in biomedical engineering or related programs; may have coursework in electronics, biology, and engineeringUsually requires certification or associate degree in biomedical technology or related field
Work EnvironmentOn-campus labs, research projects, or internships within healthcare or university settingsHospitals, clinics, or medical equipment service centers
Employer & Industry UsageEducational institutions, research labs, or healthcare facilities during studiesHealthcare providers, medical device companies, or service organizations

Work Study Biomedical Engineering Students focus on gaining academic and research experience related to biomedical engineering, often working part-time in labs or internships. Biomedical Equipment Technicians specialize in maintaining, repairing, and calibrating medical devices in clinical settings. While both roles involve medical technology, students are in training, whereas technicians are skilled professionals working in healthcare environments.

What jobs can you get with a bachelor of science in biomedical engineering?

A biomedical engineering bachelor’s degree qualifies graduates for roles such as biomedical engineer, clinical engineer, or research associate. These positions often involve designing medical devices, working in healthcare technology development, or supporting medical equipment maintenance, requiring knowledge of engineering principles and familiarity with medical standards.

Where can I work if I study biomedical engineering?

Biomedical engineering students can work in hospitals, medical device companies, research laboratories, and healthcare technology firms. These roles often involve designing, testing, and maintaining medical equipment, requiring knowledge of engineering principles and biological systems.

Where do work study biomedical engineering students work?

Work study biomedical engineering students typically work in university laboratories, research facilities, or hospital settings. They may assist with device testing, data analysis, or equipment maintenance, often gaining hands-on experience with biomedical tools and software. These positions usually require adherence to safety protocols and may involve flexible scheduling around classes.

What are popular job titles related to Work Study Biomedical Engineering Student jobs in Minnesota?

For Work Study Biomedical Engineering Student jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Work Study Biomedical Engineering Student jobs?

Cities in Minnesota with the most Work Study Biomedical Engineering Student job openings:

Infographic showing various Work Study Biomedical Engineering Student job openings in Minnesota as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 15% Part Time, and 1% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Biomedical Engineer, Design Assurance

Scanlan Int'l

Saint Paul, MN • On-site

$77K - $124K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 21 days ago


Key responsibilities

  • Represent product quality and compliance in new product development and sustaining engineering projects.

  • Develop and execute implementation, inspection, and test plans for design transfer, and support verification/validation activities.

  • Lead risk management activities such as FMEA, hazard analysis, and participate in design reviews and change control processes.


Job description

What You’ll Do: 

The Biomedical Engineer, Design Assurance, is part of the product design and development team and ensures quality and regulatory compliance throughout the medical device lifecycle for class I and II reusable surgical instruments and disposable medical devices, and supports the implementation and management of the digital requirements management system. This position reports to the Director of R&D Engineering.


40% Lead Design Assurance For Representation & Compliance

• Represent product quality and compliance in new product development and sustaining engineering projects.

• Ensure design and process controls meet regulatory and customer requirements.

• Implement medical device requirements management software (Jama) to organize and effectively manage the company’s design and development files.

• Create and update controlled documents (QSPs, specifications, methods) within the Quality Management System.


30% Product Testing

• Develop and execute implementation, inspection, and test plans for design transfer.

• Support R&D with verification/validation protocols, specifications, and reliability testing.

• Coordinate external validation activities (e.g., mechanical, functional, biocompatibility, sterilization).


20% Risk Management & Reviews

• Lead risk management activities (FMEA, hazard analysis, FTA, statistical analysis).

• Participate in design reviews and change control processes.


20% Technical Guidance & Design Principles

• Provide technical guidance on product quality attributes.

• Apply Design-to-Cost and Design-for-Manufacturability principles.


The Experience, Skills and Abilities Required: 

• Bachelor of Science in Mechanical Engineering or Biomedical Engineering

 Minimum of 3+ years design assurance or product development.

• Understanding of ISO 13485 and FDA 21 CFR 820 compliance.

• Experience with full design lifecycle and phase-gate processes.

• Understanding of FMEAs, DOEs and Risk Assessment methods

• Strong written and verbal skills for documentation, presentations, and team alignment.

• Problem-Solving & Critical Thinking: Analytical skills to identify gaps, assess risks, and draw conclusions.

• High degree of accuracy in documentation and reviews.

• Working effectively in cross-functional teams (design, manufacturing, regulatory).


Preferred Experience, Skills and Abilities:

• Experience in medical devices

• Jama Connect requirements management software

• Minitab statistical analysis software

• Knowledge of quality methodologies (Six Sigma, DFSS, DMAIC).

• Project Management, time management, prioritization, and execution.

• Leadership, mentoring, and fostering a quality culture.


This position is based out of our corporate office, south of downtown St. Paul. We welcome an on-site work environment Monday through Friday. 


Compensation

We are committed to equitable and transparent pay practices. The salary range for this position is $77,700 - $124,400, representing the minimum and maximum of our compensation structure. Starting pay will typically fall between these values and is determined based on factors such as relevant experience, skills, and internal equity. Offers near the higher end of the range are reserved for candidates with exceptional qualifications.

 

Comprehensive Benefits Offerings

- Medical, Dental, and Vision Insurance

- Group Life Insurance

- Short-Term Disability Insurance

- Long-Term Disability Insurance

- 401(k) Plan with Company Match

- Workers' Compensation

- Employee Assistance Program (EAP)

- Regular Part-Time Benefit Eligibility

- Training and Development Program

- Tuition Assistance Program

- Paid Time Off, including holidays, floating holidays, vacation and Earned Sick and Safe Time (ESST)