QC Supervisor – Medical Devices & Regulatory Excellence

Medline

Town of Hartland (WI)

On-site

USD 79,000 - 119,000

Full time

9 days ago

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Benefits offered by this job

Health insurance
401(k) contributions
Paid time off

Job summary

Medline Industries, LP seeks a dedicated QA/Quality Control leader to oversee QC functions and personnel at a distribution center. You will manage performance reviews, schedule overtime, and ensure regulatory compliance with FDA/QSR/ISO-13485 guidelines.

Responsibilities include training inspectors, coordinating with QA/Regulatory/Operations, and leading daily activities while ensuring safe material handling and occasional travel to state sites.

Qualifications

  • High school diploma or equivalent.
  • At least 3 years QC or similar experience.
  • Experience in medical device and/or drug manufacturing.
  • Intermediate knowledge of FDA/QSR/ISO-13485 guidelines.
  • Ability to lift up to 50 pounds and stand for prolonged periods.
  • Occasional/state-to-state travel.

Responsibilities

  • Oversee and manage quality control functions and personnel at designated distribution center.
  • Manage performance, attendance, monthly bonus and employee reviews for direct reports.
  • Prioritize work schedules and schedule overtime as needed.
  • Train inspectors on QSR and regulatory rules.
  • Support QA, Regulatory and Operations to ensure compliance with regulations.
  • Lead day-to-day activities, participate in hiring and performance reviews.
  • Operate material handling equipment as needed.

Skills

FDA/QSR/ISO-13485 knowledge
Regulatory compliance knowledge
People management
Travel willingness
Team leadership

Education

High school diploma or equivalent
Associates degree or technical certification preferred

Tools

Microsoft Excel
Microsoft Word

Job description

Medline Industries, LP seeks a dedicated QA/Quality Control leader to oversee QC functions and personnel at a distribution center. You will manage performance reviews, schedule overtime, and ensure regulatory compliance with FDA/QSR/ISO-13485 guidelines.

Responsibilities include training inspectors, coordinating with QA/Regulatory/Operations, and leading daily activities while ensuring safe material handling and occasional travel to state sites.

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