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Medical Device Reporting Jobs (NOW HIRING)

Medix

Medical Device Specialist

Westminster, CO · On-site

$25 - $35/hr

Generate precise diagnostic reports for review by the attending MD. * Facilitate enrollment and ... to the relevant medical personnel. * Manage the device clinic database and oversee patient ...

STAAR Surgical

Product Complaint Associate

Monrovia, CA

$25 - $32/hr

Medical Device Reports, Health Canada Reports, Vigilance reports, etc.) are submitted in compliance with respective regulations (e.g. U.S. FDA Regulations, Canadian Medical Device Regulations, MDD ...

Staar Surgical

Product Complaint Associate

Monrovia, CA · On-site

$25 - $32/hr

Medical Device Reports, Health Canada Reports, Vigilance reports, etc.) are submitted in compliance with respective regulations (e.g. U.S. FDA Regulations, Canadian Medical Device Regulations, MDD ...

DEKA

Director of Post Market Products

Manchester, NH · On-site

Deep knowledge of FDA post market requirements, including Medical Device Reporting (MDR) regulations (21 CFR Part 803), Quality System Regulation (21 CFR Part 820) / QMSR, Canada's Medical Devices ...

Intellectt INC

Medical device Assembler

Irvine, CA · On-site

$19.25 - $23.50/hr

... assembly of medical devices as well as setting up, operating, performing maintenance on and ... report to work on a regular, punctual basis. · Ability to get along with people and be able to ...

Collabera

Medical device engineer

North Chicago, IL

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Apply advanced technical writing skills to produce reports and documents; writes independently and ...

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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, Inc.

Moundsview, MN • On-site

Full-time

Posted 11 days ago

Job description

Job Title: Medical Device Complaint Specialist
Client: Med Device Manufacturing
Location: Mounds View, MN 55112
Duration: 2 Years (Possible Extension)
Shift: 1st Shift
Description:
• Review product events and determine complaint status
• Create and maintain complaint records in complaint handling systems
• Evaluate events for MDR and Vigilance reporting eligibility
• Complete and submit regulatory reports within timelines
• Conduct follow-up with internal and external contacts for missing information
• Monitor medical device surveillance and adverse event reporting activities
• Maintain accurate MDR, ADE, and vigilance documentation
• Review and analyze clinical and complaint-related databases
• Support regulatory compliance and reporting processes
• Collaborate with internal teams and external partners on reporting activities
• Assist with process improvements and project support activities
Required Skills:
• Strong analytical and critical thinking skills
• Excellent attention to detail
• Strong written and verbal communication skills
• Problem-solving and documentation abilities
• Ability to review and interpret regulatory and complaint data
• Ability to manage multiple tasks and deadlines
Preferred Skills:
• Complaint handling or MDR/Vigilance experience
• Medical device or healthcare industry experience
• Experience with regulatory reporting systems and databases
• Knowledge of FDA or medical device regulations
Education:
• Bachelor's Degree required
Work Experience:
• Experience in healthcare, medical device, complaint handling, quality, or regulatory environment preferred
• Experience with adverse event reporting or vigilance activities is a plus
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