Quality Assurance Supervisor (Pharmaceutical / USP Compliance)

About the Opportunity

Our client is a well-established North American manufacturer with a long-standing reputation for quality, innovation, and operational excellence. They are seeking a Quality Assurance Supervisor to join their team and support pharmaceutical-grade manufacturing operations at their Facility Outside Dallas, TX.

This is an excellent opportunity for a quality professional with experience in USP-regulated manufacturing who is looking to take the next step into a leadership role while working in a highly regulated production environment.

Position Overview

Reporting to the Quality Manager, the Quality Assurance Supervisor will play a key role in ensuring compliance with pharmaceutical and regulatory standards while supporting quality systems, laboratory operations, and continuous improvement initiatives.

The successful candidate will help oversee day-to-day quality activities, support regulatory audits, supervise laboratory personnel, and ensure products consistently meet customer and regulatory requirements.

Key Responsibilities

• Ensure compliance with USP specifications, GMPs, and applicable regulatory requirements.
• Support investigations of customer complaints, including root cause analysis and corrective actions.
• Assist with regulatory, customer, and internal quality audits.
• Promote and support a strong food safety and quality culture throughout the facility.
• Oversee laboratory testing, product release activities, and Good Laboratory Practices (GLP).
• Review Certificates of Analysis (COAs) and quality documentation.
• Develop, review, and maintain Standard Operating Procedures (SOPs) and quality records.
• Coordinate laboratory testing schedules with production operations.
• Lead validation studies and support continuous improvement initiatives.
• Monitor laboratory equipment calibration and maintenance.
• Review quality trends and prepare required compliance reports.
• Supervise and schedule laboratory technicians.
• Assist with employee training related to quality systems and regulatory compliance.
• Order laboratory supplies and testing equipment as required.

Qualifications

• Bachelor's degree in Chemistry, Biology, Food Science, or another related scientific discipline.
• Minimum 2 years of experience in a USP-regulated pharmaceutical manufacturing or quality laboratory environment.
• Strong understanding of pharmaceutical regulations including:
• 21 CFR Part 210
• 21 CFR Part 211
• ICH Q7
• Previous supervisory or team leadership experience is considered an asset.
• Experience conducting investigations, CAPA activities, and regulatory documentation.
• Strong organizational, analytical, and problem-solving skills.
• Excellent verbal and written communication abilities.
• Ability to work collaboratively with cross-functional teams in a fast-paced manufacturing environment.

What You'll Bring

• A proactive, self-motivated approach to quality and continuous improvement.
• Strong leadership and coaching skills.
• Excellent attention to detail and documentation practices.
• The ability to prioritize multiple projects while maintaining compliance with regulatory standards.
• A commitment to product quality, safety, and operational excellence.

Why Apply?

• Join a stable and respected manufacturing organization.
• Competitive compensation and comprehensive benefits.
• Opportunities for professional growth and advancement.
• Collaborative team environment focused on quality and continuous improvement.
• Play a key role in ensuring products meet the highest regulatory and customer standards.

Interested?

If you're an experienced quality professional with a background in pharmaceutical or USP-regulated manufacturing, we'd love to hear from you. Apply today for a confidential discussion about this opportunity.