Director of Quality Control – Regulatory Affairs

• Manage the overall operations of the Quality and Regulatory Department

• Direct and supervise lead and managerial staff

• Serve as a senior staff member supporting, educating, motivating, and directing the Quality Assurance and Regulatory Affairs team

• Ensure compliance with Good Manufacturing Practices and state, federal, and international regulatory standards

• Maintain quality standards for vendors

• Anticipate, evaluate, and control risks associated with industry and government regulations

• Ensure timely completion of team projects

• Predict, detect, estimate, and measure product defects

• Oversee labeling changes, including allergen, ingredient, warning, and nutrient-content labeling

• Develop, implement, and train staff on departmental policies and procedures

• Identify areas for improvement and quality enhancement

• Collaborate with other departments to ensure required information is available

• Manage the Quality Control Department and provide information on label reviews, vendor issues, and manufacturing changes

• Ensure drugs, dietary supplements, cosmetics, and skin-care products are manufactured, tested, stored, and distributed according to cGMP and applicable regulations

• Comply with company policies and procedures

• Perform other duties as assigned

• PhD in Chemistry or related field preferred
• 10+ years of experience in Quality Control, Pharmaceutical, Science Operations, and staff supervision
• Must work on site at the Greensboro, North Carolina offices
• Must be authorized to work without company sponsorship;
  Market America is not able to sponsor this position

Demonstrates extensive expertise in Quality Control and Regulatory Affairs, ensuring compliance with Good Manufacturing Practices and applicable regulations. Proven ability to lead and develop teams while managing quality standards and risk assessment in the pharmaceutical and dietary supplement industries.

• Quality Control Management
• Regulatory Compliance
• Team Leadership
• Good Manufacturing Practices (cGMP)
• Pharmaceutical Industry Experience

• Quality Assurance
• Risk Assessment
• Labeling Compliance
• Policy Development
• Project Management
• Defect Detection
• Vendor Management
• Staff Training
• Quality Enhancement
• Regulatory Standards

• Motivational Leadership
• Collaboration
• Communication

• Pharmaceutical
• Dietary Supplements
• Cosmetics
• Skin-Care Products
• Science Operations
• Quality Standards
• State Regulations
• Federal Regulations
• International Regulations
• Manufacturing Changes