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Entry Level Medical Device Engineer Jobs in Minnesota

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Intellectt INC

Manufacturing Engineer

Plymouth, MN · On-site

$77K - $99K/yr

... Skills): Entry-level manufacturing engineer to support the document change system (Windchill) and collaborate with engineers/operators in a medical device cleanroom environment. Must have Skills:

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Entry Level Medical Device Engineer information

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How much do entry level medical device engineer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for entry level medical device engineer in Minnesota is $30.67, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $33.89 per hour, depending on experience, location, and employer.

What does an entry level medical device engineer do?

An entry level medical device engineer assists in designing, developing, and testing medical devices such as implants, diagnostic equipment, or surgical tools. They often work as part of a team under the supervision of experienced engineers, ensuring products meet regulatory standards and function safely and effectively. Responsibilities may also include documenting results, conducting research, and supporting manufacturing or quality assurance processes. This role provides hands-on experience with engineering principles in the healthcare industry and often serves as a starting point for more specialized or senior positions.

What is the difference between Entry Level Medical Device Engineer vs Quality Assurance Technician?

AspectEntry Level Medical Device EngineerQuality Assurance Technician
Required CredentialsBachelor's in engineering, biomedical or related fieldBachelor's in science, engineering, or related field; certifications optional
Work EnvironmentDesign labs, manufacturing facilities, R&D teamsManufacturing plants, quality control labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, healthcare device companies

Entry Level Medical Device Engineers focus on designing and developing medical devices, while Quality Assurance Technicians ensure products meet quality standards. Both roles are essential in the medical device industry and often work closely to ensure product safety and compliance.

What Does an Entry-Level Medical Device Engineer Do?

As an entry-level medical device engineer, your duties include the research, design, and development of medical devices and healthcare products and equipment. An entry-level engineer works as part of a research and development team. You typically have specific tasks such as performing research on materials or testing a device in a laboratory setting or during a clinical trial. In addition to responsibilities related to design and development, entry-level engineers often document tests and trials, collect and organize data, and create drawings and plans using computer-aided design software.

What types of projects and responsibilities can an entry level medical device engineer expect during their first year on the job?

As an entry level medical device engineer, you can expect to work closely with cross-functional teams—including design, quality, and manufacturing—to support product development and improvements. Your responsibilities may include assisting in prototyping, conducting testing and data analysis, and maintaining detailed documentation to ensure regulatory compliance. You’ll likely gain hands-on experience troubleshooting devices, collaborating in design reviews, and participating in validation activities. This role provides an excellent foundation for learning industry standards and building technical and teamwork skills essential for career advancement.

What are the key skills and qualifications needed to thrive as an Entry Level Medical Device Engineer, and why are they important?

To thrive as an Entry Level Medical Device Engineer, you need a bachelor's degree in biomedical, mechanical, or electrical engineering, along with a solid understanding of engineering principles and medical device regulations. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO standards is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you stand out in this role. These competencies are critical for ensuring the safe design and development of innovative medical devices that meet regulatory standards and patient needs.
More about Entry Level Medical Device Engineer jobs
What are the most commonly searched types of Medical Device Engineer jobs in Minnesota? The most popular types of Medical Device Engineer jobs in Minnesota are:
What are popular job titles related to Entry Level Medical Device Engineer jobs in Minnesota? For Entry Level Medical Device Engineer jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Entry Level Medical Device Engineer jobs in Minnesota look for? The top searched job categories for Entry Level Medical Device Engineer jobs in Minnesota are:
What cities in Minnesota are hiring for Entry Level Medical Device Engineer jobs? Cities in Minnesota with the most Entry Level Medical Device Engineer job openings:
Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer job openings in Minnesota as of July 2026, with employment types broken down into 74% Full Time, 18% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $63,789 per year, or $30.7 per hour.
Medical Device Complaint Specialist

Medical Device Complaint Specialist

Three Point Solutions, Inc.

Moundsview, MN • On-site

Full-time

Posted 27 days ago

Job description

Job Title: Medical Device Complaint Specialist
Client: Medical Device Manufacturing Company
Location: Mounds View, MN 55112
Duration: 12 Months (Possible Extension)
Shift: 1st Shift
Job Summary
Entry-level medical device safety and complaint investigation role responsible for intake, documentation, adverse event reporting, MDR submissions, and vigilance activities for Neurovascular products while ensuring compliance with regulatory requirements.
Key Responsibilities
• Review, document, and investigate product complaints
• Process Medical Device Reports (MDRs) and adverse event cases
• Maintain accurate complaint and vigilance records
• Analyze safety and clinical data for reporting purposes
• Ensure compliance with FDA and global regulatory requirements
• Support complaint investigations and follow-up activities
• Collaborate with cross-functional teams and external partners
• Assist with process improvements and quality initiatives
• Prepare regulatory documentation and reports
Core Duties
• Complaint handling & investigation
• Medical Device Reporting (MDR)
• Adverse event processing
• Regulatory compliance support
• Safety data review & analysis
• Documentation & case management
Required Skills
• Critical thinking and decision-making
• Strong attention to detail
• Excellent written and verbal communication
• Investigation and problem-solving skills
• Documentation and record management
• Organization and time management
Preferred Skills
• Medical device industry experience
• Pharmaceutical industry experience
• Complaint handling experience
• Regulatory reporting knowledge
• Quality or compliance exposure
• Clinical data review experience
Technical / Functional Exposure
• Medical Device Reporting (MDR)
• Vigilance & Post-Market Surveillance
• Complaint Investigation
• Adverse Event Reporting (ADE)
• Regulatory Compliance
• Clinical & Safety Data Analysis
Work Environment
• Medical device regulatory and quality environment
• Cross-functional collaboration with quality, regulatory, and clinical teams
• Process-driven and compliance-focused role
• Training and development opportunities for entry-level professionals
Education / Experience
• Bachelor's Degree in Bio-Sciences, Engineering, Life Sciences, or related field required
• Experience in Medical Device, Pharmaceutical, Quality, Regulatory, Clinical, or related industry
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