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Commission Complaint Handling Medical Device Jobs

Masimo

Clinical Complaint Specialist

Irvine, CA · On-site

$80K - $100K/yr

Experience in the medical device, biotechnology, pharmaceutical, diagnostics, or healthcare industry. * Experience with complaint handling, adverse event reporting, post-market surveillance, or ...

Masimo

Clinical Complaint Specialist

Irvine, CA

$80K - $100K/yr

Experience in the medical device, biotechnology, pharmaceutical, diagnostics, or healthcare industry. * Experience with complaint handling, adverse event reporting, post-market surveillance, or ...

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How much do commission complaint handling medical device jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for commission complaint handling medical device in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What is the difference between Commission Complaint Handling Medical Device vs Medical Device Quality Assurance Specialist?

AspectCommission Complaint Handling Medical DeviceMedical Device Quality Assurance Specialist
CertificationsRegulatory compliance, complaint management trainingISO 13485, GMP, quality systems training
Work EnvironmentCustomer service, regulatory agencies, complaint investigationsManufacturing facilities, quality departments, audits
Employer & Industry UsageMedical device companies, regulatory bodiesManufacturers, quality assurance departments
Search & Comparison IntentUnderstanding complaint processes, regulatory rolesQuality assurance procedures, compliance standards

The Commission Complaint Handling Medical Device role focuses on managing and investigating complaints related to medical devices, ensuring regulatory compliance and customer safety. In contrast, a Medical Device Quality Assurance Specialist concentrates on maintaining quality standards, conducting audits, and ensuring products meet industry regulations. While both roles require knowledge of medical device regulations, complaint handling emphasizes customer issues and regulatory reporting, whereas quality assurance emphasizes product quality and process improvements.

What cities are hiring for Commission Complaint Handling Medical Device jobs? Cities with the most Commission Complaint Handling Medical Device job openings:
What are the most commonly searched types of Complaint Handling Medical Device jobs? The most popular types of Complaint Handling Medical Device jobs are:
What states have the most Commission Complaint Handling Medical Device jobs? States with the most job openings for Commission Complaint Handling Medical Device jobs include:
Commission Complaint Handling Medical Device jobs near you

Medical Device Complaint Specialist

Three Point Solutions

Moundsview, MN • On-site

$25 - $27/hr

Contractor

Re-posted 18 days ago

Job description

Job Title:         Medical Device Complaint Specialist

Client:              Medical Device Manufacturing Company

Duration:         2 Years (Possible Extension)

Location:         Mounds View, MN 55112

Shift:                1st Shift

Key Responsibilities

  • Review and evaluate product complaints and adverse event reports.
  • Determine Medical Device Reporting (MDR) and Vigilance reporting eligibility.
  • Prepare and submit MDR, Vigilance Reports (VR), and Adverse Drug Experience (ADE) reports.
  • Monitor complaint investigations through closure and ensure timely follow-up.
  • Review product analysis and investigation results.
  • Ensure compliance with FDA and international (OUS) regulatory requirements.
  • Maintain complaint documentation and regulatory records.
  • Analyze clinical and safety data for regulatory reporting.
  • Collaborate with internal teams and external partners to collect complaint information.
  • Support medical device surveillance and post-market vigilance activities.
  • Maintain knowledge of new products, regulations, and reporting requirements.
  • Support continuous improvement of complaint handling and regulatory reporting processes.

Must-Have Requirements

  • Bachelor's Degree in a Science-related field.
  • 1–2 years of experience in Healthcare, Medical Device, Pharmaceutical, Safety, or Clinical Data Evaluation.
  • Strong computer skills (Microsoft Office, SAP, Siebel, Oracle Clinical, or similar systems).
  • Knowledge of complaint handling and adverse event documentation.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.
  • High attention to detail.
  • Ability to work with regulatory documentation and confidential information.

Preferred Qualifications

  • Degree in Nursing, Biology, Pre-Med, Pre-Vet, Biomedical Engineering, or Biomedical Sciences.
  • Clinical or nursing background.
  • Medical Device industry experience.
  • Knowledge of FDA Medical Device Reporting (MDR) requirements.
  • Knowledge of anatomy and physiology.
  • Experience with complaint investigations and post-market surveillance.
  • Experience with regulatory reporting systems.

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