Quality Control Supervisor: Lead Cleanroom QC Team

EuroMed, Inc.

Orangeburg (NY)

On-site

USD 85,000 - 120,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, and vision insurance
401(k) with company match
Paid vacation and personal time off
Career development support

Job summary

Mativ is seeking a Quality Control Supervisor to lead QC Inspectors in cleanroom environments, ensuring adherence to procedures and safe manufacturing practices. You will oversee staffing, training, timekeeping, and performance reviews to uphold quality standards.

This role requires 5+ years in quality, experience with GMP/ISO concepts, and strong documentation discipline. You will collaborate with Production and HR, drive continuous improvement, and maintain IQS/Epicor systems relevant to

Qualifications

  • Minimum 5 years in quality, preferably in medical device/drug manufacturing.
  • Reading technical docs and basic GD&T understanding.
  • Proficient with inspection equipment and documentation.
  • Experience leading or supervising personnel.

Responsibilities

  • Oversee QC Inspectors in cleanroom and carton areas.
  • Schedule workload and approve time cards / PTO.
  • Train staff and enforce policies with HR coordination.
  • Maintain quality records and drive corrective actions.
  • Lead root cause analysis and coordinate with Production.
  • Ensure safety and adherence to procedures across shifts.

Skills

Team leadership
Quality control
Documentation
Cleanroom experience
Training
Root cause analysis

Education

High school diploma
ASQ certification

Tools

Epicor
IQS

Job description

Mativ is seeking a Quality Control Supervisor to lead QC Inspectors in cleanroom environments, ensuring adherence to procedures and safe manufacturing practices. You will oversee staffing, training, timekeeping, and performance reviews to uphold quality standards.

This role requires 5+ years in quality, experience with GMP/ISO concepts, and strong documentation discipline. You will collaborate with Production and HR, drive continuous improvement, and maintain IQS/Epicor systems relevant to

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