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Quality Assurance Supervisor

Job in Tyler, Smith County, Texas, 75713, USA
Listing for: T. Burks & Associates
Full Time position
Listed on 2026-07-03
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
  • Pharmaceutical
    Regulatory Compliance Specialist
Job Description & How to Apply Below

Quality Assurance Supervisor

We are hiring a Quality Assurance Supervisor to support site-level compliance with USP standards, FDA pharmaceutical regulations, current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and internal quality systems.

This role provides day-to-day leadership for laboratory operations, quality systems, and regulatory compliance. The ideal candidate has experience working in a pharmaceutical, nutraceutical, OTC drug, API, or other FDA-regulated manufacturing environment and understands the regulatory expectations surrounding USP-compliant products.

Key Responsibilities

  • Ensure compliance with USP standards, FDA regulations, cGMP, GLP, and customer requirements.
  • Oversee USP laboratory testing, product release, COA review, equipment calibration, and validation activities.
  • Lead investigations, root cause analysis, CAPA, and quality trend reporting.
  • Support FDA inspections, regulatory audits, and customer audits.
  • Develop and maintain USP-related SOPs, work instructions, and quality documentation.
  • Supervise and schedule USP Technicians and coordinate testing with operations.
  • Promote a culture of quality, compliance, and continuous improvement.

Required

  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Food Science, or a related science field.
  • 2+ years of quality experience in pharmaceutical, OTC drug, nutraceutical, API, or other FDA-regulated manufacturing environments.
  • Strong knowledge of USP standards, FDA 21 CFR Parts 210 & 211, cGMP, GLP, CAPA, validation, and quality systems.

Preferred

  • Supervisory experience.
  • Experience with FDA inspections, ICH guidelines, and validation programs.
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