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Medical Device Reporting Jobs in Minnesota (NOW HIRING)

Collabera

Vigilance Specialists

Minneapolis, MN · On-site

Associate MDR/Vigilance Specialists are responsible for theintake, documentation, Medical Device Reporting, and investigation of complaintsfor legacy Neuromodulation products in accordance with ...

Three Point Solutions, Inc.

Medical Assembler

Brooklyn Park, MN · On-site

$18.75 - $23/hr

Medical Device Manufacturing Company Duration : 12 Months Location : Brooklyn Park, MN 55445 Shift ... Report material shortages to supervisors. * Maintain a clean and safe work area. * Follow GMP, GDP ...

Abbott

Product Performance Analyst I

Saint Paul, MN

$50K - $101K/yr

Knowledge of global regulations for medical device reporting and medical terminology is a plus. * Strong written and oral communication skills are required. * Candidates must be able to work well ...

Abbott

Product Performance Analyst I

Saint Paul, MN · On-site

$50K - $101K/yr

Knowledge of global regulations for medical device reporting and medical terminology is a plus. * Strong written and oral communication skills are required. * Candidates must be able to work well ...

Abbott

Product Performance Analyst I

Saint Paul, MN · On-site

$50K - $101K/yr

Knowledge of global regulations for medical device reporting and medical terminology is a plus. * Strong written and oral communication skills are required. * Candidates must be able to work well ...

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All JobsMedical Device Reporting JobsMedical Device Reporting Jobs in Minnesota

Medical Device Reporting information

See Minnesota salary details

$12

$19

$25

How much do medical device reporting jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical device reporting in Minnesota is $19.22, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $20.72 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Reporting vs Medical Device Technician?

AspectMedical Device ReportingMedical Device Technician
Required CredentialsRegulatory knowledge, often a background in healthcare or regulatory affairsTechnical skills, certifications in medical equipment maintenance or biomedical technology
Work EnvironmentRegulatory agencies, healthcare compliance departmentsHospitals, clinics, biomedical equipment service centers
Employer & Industry UsageUsed by medical device manufacturers, healthcare providers, and regulatory bodiesEmployers include hospitals and biomedical service companies
Common Search & Comparison IntentUnderstanding regulatory roles in medical device safetyTechnical maintenance and repair of medical devices

Medical Device Reporting focuses on regulatory compliance and reporting adverse events, while Medical Device Technicians handle the maintenance and repair of medical equipment. Both roles are essential in the medical device industry but serve different functions within healthcare and regulatory environments.

What are the key skills and qualifications needed to thrive in medical device reporting, and why are they important?

To excel in Medical Device Reporting, you need a solid understanding of regulatory requirements, data analysis, and healthcare compliance, often supported by a degree in life sciences or a related field. Familiarity with regulatory databases such as FDA’s MAUDE, electronic reporting systems, and quality management software is typically required. Strong attention to detail, analytical thinking, and effective written communication help ensure accurate and timely reporting. These skills are critical for maintaining regulatory compliance, protecting patient safety, and supporting product quality in the medical device industry.

What are some typical challenges faced by professionals in medical device reporting, and how can they be managed?

Professionals working in Medical Device Reporting often encounter challenges such as managing tight regulatory deadlines, ensuring complete and accurate documentation, and staying current with evolving global reporting requirements. Effective time management, attention to detail, and regular training on regulatory updates are essential for success in this role. Collaboration with quality assurance, regulatory affairs, and clinical teams also helps ensure timely and compliant submissions, minimizing the risk of non-compliance.

What is medical device reporting?

Medical device reporting is the process by which manufacturers, importers, and device user facilities notify regulatory authorities, such as the FDA, about certain adverse events and product problems involving medical devices. This reporting system helps monitor the safety and effectiveness of medical devices once they are on the market. The information collected can lead to recalls, safety alerts, or other actions to protect public health.
What are popular job titles related to Medical Device Reporting jobs in Minnesota? For Medical Device Reporting jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Medical Device Reporting jobs in Minnesota look for? The top searched job categories for Medical Device Reporting jobs in Minnesota are:
What cities in Minnesota are hiring for Medical Device Reporting jobs? Cities in Minnesota with the most Medical Device Reporting job openings:
Medical Device Reporting jobs near you
Infographic showing various Medical Device Reporting 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 $39,972 per year, or $19.2 per hour.

Medical Device Complaint Specialist

Three Point Solutions, Inc.

Moundsview, MN • On-site

Full-time

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
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