×
Register Here to Apply for Jobs or Post Jobs. X
More jobs:

Complaints Handler

Job in Vernon Hills, Lake County, Illinois, 60061, USA
Listing for: Stellar Consulting Solutions, LLC
Full Time position
Listed on 2025-10-31
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 38 - 40 USD Hourly USD 38.00 40.00 HOUR
Job Description & How to Apply Below

Stellar Consulting Solutions, LLC provided pay range

This range is provided by Stellar Consulting Solutions, LLC. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$38.00/hr - $40.00/hr

Job Title:
Quality Systems Specialist-Complaints Handling

Location:
Vernon Hills, IL Hybrid (2 days onsite, remainder remote)

Duration: 9+Months

Job Summary

The Quality Systems Specialist supports the company’s Quality Management System (QMS) by managing customer complaints, ensuring compliance with FDA and ISO regulations, and contributing to continuous improvement in product quality and customer satisfaction.

Key Responsibilities

  • Apply Quality System standards consistently across assigned areas.
  • Manage the end-to-end customer complaint process, including review, investigation, documentation, and response.
  • Conduct root cause analyses and recommend corrective/preventive actions (CAPA).
  • Identify and track complaint trends to support product and process improvements.
  • Prepare investigation reports and complaint closure letters.
  • Review and validate all complaints for compliance with internal policies and regulatory requirements.
  • Determine if complaints meet Medical Device Reporting (MDR) criteria and prepare Med Watch reports when applicable.
  • Collaborate with Regional Complaint Centers and cross-functional teams to resolve issues.
  • Use complaint databases (e.g., Track Wise) and develop quality metrics and reports.
  • Provide internal guidance and training on complaint handling and regulatory compliance.
  • Support internal and cross-business quality projects and continuous improvement initiatives.

Qualifications

  • Education: Bachelor’s degree (preferred in Clinical, Science, or Engineering field).
  • Experience: 2–3 years in Quality Systems, Regulatory Affairs, or related medical device/pharma industry role.
  • Working knowledge of FDA and ISO quality system regulations.
  • Experience with complaint handling systems (Track Wise preferred).
  • Proficiency in Microsoft Excel, Word, and PowerPoint.
  • Strong analytical, communication, and problem-solving skills.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary