Quality Assurance Supervisor & Compliance Lead

International Vitamin Corporation

South Carolina

On-site

USD 90,000 - 130,000

Full time

14 days+

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Job summary

International Vitamin Corporation (IVC) is seeking an experienced QA Supervisor to oversee finished product and packaging component inspection/release activities. The role ensures adherence to GMP, FDA quality systems, and 21 CFR standards, while mentoring staff and driving continuous improvement across the QA function.

The candidate should have a strong background in quality systems within dietary supplements or pharmaceutical manufacturing, with 3+ years in supervisory roles, and a proven

Qualifications

  • Bachelor’s Degree in a Scientific or Engineering discipline with exposure to Chemistry, Microbiology, and/or Biology.
  • Professional quality discipline certifications (CQE, CQA, CQM or RAB) desired.
  • Minimum 5–10 years of experience establishing and maintaining quality systems in dietary supplements/pharma manufacturing with 3+ years in supervision.

Responsibilities

  • Manage tactical execution of short- and long-term objectives with direct responsibility for results, including cost, methods, and staffing.
  • Provide leadership, coaching and development plans for direct reports; partner with HR on employee matters.
  • Involve in the development, modification and execution of company policies affecting operations.
  • Implement strategic policies for methods, techniques and evaluation criteria to obtain results.
  • Establish objectives and metrics aligned to goals and department/programs.

Skills

Communication
Negotiation
CRM software
Microsoft Office
Attention to detail
Account management
Relationship building
Time management
Adaptability
Data analysis
Regulatory knowledge

Education

Bachelor’s Degree in Science/Engineering
CQE/CQA/CQM or RAC certification desired
Professional quality certifications (CQMOE, CQE, CQA, RAC) desired

Tools

CRM software
Microsoft Office

Job description

International Vitamin Corporation (IVC) is seeking an experienced QA Supervisor to oversee finished product and packaging component inspection/release activities. The role ensures adherence to GMP, FDA quality systems, and 21 CFR standards, while mentoring staff and driving continuous improvement across the QA function.

The candidate should have a strong background in quality systems within dietary supplements or pharmaceutical manufacturing, with 3+ years in supervisory roles, and a proven

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