ZipRecruiter

Log In

1

Medical Device Analyst Jobs in Minnesota (NOW HIRING)

next page

Showing results 1-20

All JobsMedical Device Analyst JobsMedical Device Analyst Jobs in Minnesota

Medical Device Analyst information

See Minnesota salary details

$30.4K

$71.8K

$127.3K

How much do medical device analyst jobs pay per year?

As of Aug 10, 2026, the average yearly pay for medical device analyst in Minnesota is $71,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,400.00 and $85,200.00 per year, depending on experience, location, and employer.

Is a medical device analyst a good career?

A medical device analyst is a viable career option for those interested in healthcare technology, involving tasks such as evaluating device performance, ensuring regulatory compliance, and supporting product development. It typically requires knowledge of medical regulations, data analysis skills, and familiarity with industry standards, offering opportunities for growth in the medical device industry.

What is a medical device analyst?

A medical device analyst evaluates and monitors medical devices to ensure they meet safety, quality, and regulatory standards. They often review clinical data, perform risk assessments, and stay updated on industry regulations, typically requiring knowledge of healthcare regulations and proficiency with data analysis tools.

What does a medical device analyst do?

A Medical Device Analyst evaluates, tests, and ensures compliance of medical devices with industry regulations and safety standards. They analyze data, assess product performance, and collaborate with regulatory teams to meet market requirements. Their role often involves reviewing risk assessments, troubleshooting device issues, and supporting the development of new medical technologies. Strong analytical skills and knowledge of medical regulations, such as FDA and ISO guidelines, are essential.

What are the key skills and qualifications needed to thrive as a medical device analyst?

A Medical Device Analyst requires strong analytical skills, attention to detail, and a background in biomedical engineering or a related field, often supported by a bachelor's degree. Familiarity with regulatory standards (such as FDA or ISO), proficiency with data analysis tools, and experience using quality management systems are typically necessary. Excellent problem-solving abilities, effective communication skills, and collaborative teamwork are valuable soft skills in this role. These competencies ensure accurate evaluation, compliance, and the ability to convey findings clearly, supporting safe and effective medical device development.

What are popular job titles related to Medical Device Analyst jobs in Minnesota? For Medical Device Analyst jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Medical Device Analyst jobs in Minnesota look for? The top searched job categories for Medical Device Analyst jobs in Minnesota are:
What cities in Minnesota are hiring for Medical Device Analyst jobs? Cities in Minnesota with the most Medical Device Analyst job openings:
Medical Device Analyst jobs near you
Infographic showing various Medical Device Analyst job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $71,753 per year, or $34.5 per hour.

Medical Device Complaint Specialist

Three Point Solutions

Moundsview, MN • On-site

$24 - $27/hr

Contractor

Re-posted 22 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

#ZR