More jobs:
Complaints Handler
Job in
Vernon Hills, Lake County, Illinois, 60061, USA
Listed on 2025-10-31
Listing for:
Stellar Consulting Solutions, LLC
Full Time
position Listed on 2025-10-31
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Data Scientist
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.
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