ZipRecruiter

Log In

1

Medical Device Reporting Jobs (NOW HIRING)

Lancesoft INC

Assembly (Medical device)

Durham, NC · On-site

$18 - $18.20/hr

Report production or equipment issues to supervisors Qualifications * High school diploma or GED ... Medical device or manufacturing assembly experience * Experience using measuring tools or ...

DEKA

Product Complaints Engineer

Manchester, NH · On-site

Identify and make sound decisions regarding medical device reporting to regulatory agencies. * Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory ...

next page

Showing results 1-20

People also search for

All JobsMedical Device Reporting Jobs

Medical Device Reporting information

See salary details

$12

$19

$25

How much do medical device reporting jobs pay per hour?

As of May 31, 2026, the average hourly pay for medical device reporting in the United States is $19.62, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $21.15 per hour, depending on experience, location, and employer.

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 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.

More about Medical Device Reporting jobs
What cities are hiring for Medical Device Reporting jobs? Cities with the most Medical Device Reporting job openings:
What states have the most Medical Device Reporting jobs? States with the most job openings for Medical Device Reporting jobs include:
What job categories do people searching Medical Device Reporting jobs look for? The top searched job categories for Medical Device Reporting jobs are:
Medical Device Reporting jobs near you
Infographic showing various Medical Device Reporting job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 75% Physical, 4% Hybrid, and 21% Remote job distribution, with an average salary of $40,813 per year, or $19.6 per hour.
Medical Device Complaint Specialist

Medical Device Complaint Specialist

Three Point Solutions

Moundsview, MN • On-site

$25 - $27/hr

Contractor

Posted 10 days ago

Job description

Job Title:         Medical Device Complaint Specialist
Client:              Medical Device Manufacturing Company
Location:         Mounds View, MN 55112
Duration:         24 Months (Possible Extension)
Shift:                1st Shift

Job Summary

Supports medical device safety and regulatory compliance by evaluating product complaints, determining reporting requirements, and ensuring accurate submission of regulatory reports (MDR/Vigilance).

Key Responsibilities

  • Review product complaints and determine regulatory reporting eligibility
  • Prepare and submit Medical Device Reports (MDRs) and Vigilance Reports
  • Monitor complaint lifecycle to ensure timely closure
  • Collaborate with internal teams for data collection and investigation

Core Duties

  • Evaluate adverse event data and product feedback
  • Analyze clinical and product data for safety reporting
  • Maintain compliance with FDA and global (OUS) regulations
  • Support complaint investigations and follow-ups
  • Ensure accuracy and completeness of regulatory documentation
  • Act as liaison across teams for compliance and reporting processes

Required Qualifications

  • Bachelor’s degree (Biology, Nursing, Biomedical, Pre-med/Pre-vet preferred)
  • 0–2 years experience (entry-level acceptable)
  • Strong understanding of anatomy/physiology (academic is fine)
  • High attention to detail and analytical thinking
  • Proficiency in MS Office and data systems (SAP, Oracle, etc.)

Preferred Qualifications

  • Clinical or medical device exposure
  • Strong written and verbal communication skills
  • Experience in safety, clinical data, or regulatory environments

Key Skills

  • Regulatory compliance & documentation
  • Data analysis & interpretation
  • Attention to detail (critical for reporting accuracy)
  • Cross-functional coordination
  • Problem identification & resolution

#ZR