Quality Assurance Supervisor

T. Burks & Associates

Tyler, TX

JOB DETAILS
SKILLS
Active Pharmaceutical Ingredient (API), Biology, Biotech and Pharmaceutical, Calibration, Chemistry, Code of Federal Regulations, Continuous Improvement, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Documentation, Equipment Validation, FDA (Food and Drug Administration), FDA Requirements, Food Science, GLP (Good Laboratory Practices), ICH Regulations, Laboratory Management, Laboratory Operations, Laboratory Testing, Leadership, Maintain Compliance, Manufacturing, People Management, Product Testing, Quality Assurance, Quality Management, Regulations, Regulatory Compliance, Root Cause Analysis, Schedule Development, Standard Operating Procedures (SOP), Trend Analysis
LOCATION
Tyler, TX
POSTED
1 day ago
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.

About the Company

T

T. Burks & Associates