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Job description
• 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
Requirements
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
Core Competencies
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.
Highest-signal resume keywords
Quality Control Management
Regulatory Compliance
Team Leadership
Good Manufacturing Practices (cGMP)
Pharmaceutical Industry Experience
ATS Optimization Keywords
Hard Skills
Quality Assurance
Risk Assessment
Labeling Compliance
Policy Development
Project Management
Defect Detection
Vendor Management
Staff Training
Quality Enhancement
Regulatory Standards
Soft Skills
Motivational Leadership
Collaboration
Communication
Industry Keywords
Pharmaceutical
Dietary Supplements
Cosmetics
Skin-Care Products
Science Operations
Quality Standards
State Regulations
Federal Regulations
International Regulations
Manufacturing Changes
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Worksite address
greensboro, NC, 27497, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.