Director, Quality Control & GMP Compliance

Medivant Healthcare; Chandler, Northern (AZ, KY); Hybrid; USD 130,000 - 140,000; Full time

Job summary

Medivant Healthcare in Chandler, AZ seeks a Director of Quality Control to lead QC Analytical Chemistry and Microbiology for sterile injectable manufacturing, ensuring GMP compliance, inspections readiness, and continuous improvement.

The role oversees testing, product release, investigations, data integrity, environmental monitoring, and overall laboratory operations—driving performance, quality, and regulatory readiness across the QC organization.

Qualifications

• Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or related discipline.
• 10+ years of QC experience in pharmaceutical manufacturing.
• 5+ years of leadership experience in GMP-regulated laboratories.
• Strong experience with sterile injectables, analytical testing, microbiology, and environmental monitoring.
• In-depth knowledge of FDA, USP, GMP, and data integrity requirements.
• Experience supporting regulatory inspections and audits.

Responsibilities

• Lead QC Analytical Chemistry and Microbiology laboratories.
• Manage budgets, staffing, laboratory capacity, and capital investments.
• Establish QC KPIs and drive operational excellence.
• Recruit, mentor, and develop laboratory personnel.
• Promote a culture of quality, accountability, and continuous improvement.
• Oversee testing and product release timelines and batch release support.

Skills

Leadership

QC Leadership

Analytical testing

Regulatory knowledge

Data integrity

Cross-functional collaboration

Education

Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences

Job description

Medivant Healthcare in Chandler, AZ seeks a Director of Quality Control to lead QC Analytical Chemistry and Microbiology for sterile injectable manufacturing, ensuring GMP compliance, inspections readiness, and continuous improvement.

The role oversees testing, product release, investigations, data integrity, environmental monitoring, and overall laboratory operations—driving performance, quality, and regulatory readiness across the QC organization.