top of page
Food and Beverage Recruiters Minnesota.webp
Manufacturing leader.webp
Industrial Automation.webp

Customer Quality & Complaint Specialist

Monroe Township, NJ

Job ID

8358

Opening Type

Existing Vacancy

Workspace

On-Site

Industry

Date Posted

Medical Device

July 24, 2026

About the Role

The Customer Quality & Complaint Specialist will be responsible for managing customer quality concerns, investigating product complaints, coordinating corrective and preventive actions (CAPA), and ensuring customer satisfaction through timely resolution of quality-related issues.

Key Activities

  • Manage day-to-day customer service activities, including product inquiries, customer support, issue resolution, and follow-up.

  • Coordinate activities with third-party customer service vendors, including ARS and outsourced call centre providers.

  • Maintain customer service procedures and monitor vendor service level agreements (SLAs).

  • Ensure customer inquiries are handled accurately, professionally, and within established response timelines.

  • Maintain complete and accurate records of customer communications and service activities.

  • Track customer service performance metrics and prepare periodic reports for management.

  • Identify opportunities to improve customer service processes and overall customer experience.

  • Receive, review, document, and process customer complaints in accordance with Company procedures and applicable regulatory requirements.

  • Evaluate customer feedback to determine whether it meets the definition of a product complaint.

  • Coordinate complaint investigations with Quality Assurance, Regulatory Affairs, Manufacturing, Engineering, R&D, and other cross-functional teams.

  • Maintain complete and accurate complaint records and ensure timely processing and closure.

  • Escalate complaints requiring further Quality review, including CAPA, Risk Management, or MDR evaluation, as appropriate.

  • Support complaint trend analysis to identify recurring quality issues and opportunities for improvement.

  • Maintain complaint files and related documentation in accordance with document control procedures.

  • Manage day-to-day communication with outsourced customer service vendors and call centre providers.

  • Monitor vendor performance using established KPIs and service level agreements.

  • Conduct periodic vendor performance reviews and follow up on corrective or improvement actions.

  • Ensure vendors follow approved customer service and complaint handling procedures.

  • Coordinate training and communications with vendor personnel regarding customer service and complaint handling processes.

  • Support preparation of complaint-related documentation for FDA inspections, ISO 13485 audits, internal and customer audits.

  • Support complaint trending, data analysis, and post-market quality activities. · Participate in CAPA activities and Management Review by preparing complaint and customer service performance data.

Preferred Skills

  • Experience with medical device complaint handling, customer quality, or Quality Management System (QMS) processes.

  • Familiarity with FDA Quality System requirements, ISO 13485, CAPA, or post-market surveillance.

  • Experience using CRM, complaint management, or QMS software.

Education and Experience

  • Bachelor’s degree in Business Administration, Life Sciences, Healthcare, Engineering, Quality, or a related field.

  • 3–5 years of experience in customer service, customer support, or customer relationship management, preferably in a healthcare or other regulated industry.

  • Experience handling customer inquiries, issue resolution, and communication with internal and external stakeholders.

  • Experience coordinating with external service providers or customer service vendors.

About Us

Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible.    


TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.    
   
Accommodation for applicants with disabilities is available upon request.    

Apply for Role

Please complete the form to apply for a position with us.

Upload File
Upload supported file (Max 15MB)

Thanks for submitting!

bottom of page