Quality Control Supervisor: Lead QC Team on the Floor

Biovation Labs LLC

Salt Lake City (UT)

On-site

USD 60,000 - 70,000

Full time

24 hours ago
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Job summary

Biovation Labs LLC is seeking a Quality Supervisor to lead the Quality Control team in Salt Lake City, ensuring effective oversight of QC technicians and daily quality activities on the production floor.

The role emphasizes maintaining cGMP compliance, reviewing documentation, and supporting investigations and corrective actions across shifts. Collaboration with Production and other departments is essential to meet regulatory and quality standards.

Qualifications

  • High school diploma or GED required; associate or bachelor’s degree in science, quality, manufacturing, or related field preferred.
  • Experience in quality control or quality assurance in a regulated manufacturing environment is required or preferred.
  • Strong knowledge of cGMPs and 21 CFR Part 111 compliance.

Responsibilities

  • Provide front-line leadership for Quality Control Technicians during shifts and ensure coverage.
  • Oversee production-floor QC activities including inspections, dispositions, and documentation.
  • Coach and develop QC staff and participate in performance evaluations and training.
  • Support investigations, deviations, CAPA, and root-cause analysis with cross-functional teams.
  • Collaborate with Production, Warehouse, Maintenance, and other Quality functions to resolve issues.
  • Ensure compliance with FDA requirements, safety, and company quality standards across shifts.

Skills

Leadership
cGMP knowledge
Quality control
Process improvement
Regulatory audits
Problem solving
Communication
Team coaching

Education

High school diploma or GED
Associate or Bachelor’s degree in science/quality/manufacturing

Tools

Microsoft Excel
Microsoft Word
Outlook
Documentation systems

Job description

Biovation Labs LLC is seeking a Quality Supervisor to lead the Quality Control team in Salt Lake City, ensuring effective oversight of QC technicians and daily quality activities on the production floor.

The role emphasizes maintaining cGMP compliance, reviewing documentation, and supporting investigations and corrective actions across shifts. Collaboration with Production and other departments is essential to meet regulatory and quality standards.

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