Multisite Quality Compliance & Audit Lead

International Vitamin Corporation; Greenville (SC); On-site; USD 85,000 - 105,000; Full time

Job summary

International Vitamin Corporation seeks a Sr. Quality Compliance Specialist to lead internal and external audits across multiple sites. You will manage the audit program, coordinate CAPAs, and ensure regulatory alignment with cGMP requirements for dietary supplements.

The role requires strong documentation, cross-functional collaboration, and ability to respond swiftly to inspection findings while maintaining audit records and continuous improvement initiatives.

Qualifications

• Experience coordinating internal and external audits.
• Knowledge of FDA 21 CFR Part 111 (Dietary Supplement cGMPs) is preferred.
• Experience managing audit responses, CAPAs, and audit documentation.

Responsibilities

• Develop, implement, and maintain internal audit program across four sites.
• Coordinate annual audit schedule and lead audit teams.
• Serve as QA point of contact for external audits and logistics.
• Manage audit-day documentation requests and timely responses.
• Prepare and submit audit responses and CAPA-related findings.

Skills

Audit Management

CAPA

Documentation

Quality Assurance

Regulatory Compliance

FDA inspections

Multi-site coordination

Internal Auditor

Education

Bachelor's degree in Quality or related field

Tools

QMS software

Job description

International Vitamin Corporation seeks a Sr. Quality Compliance Specialist to lead internal and external audits across multiple sites. You will manage the audit program, coordinate CAPAs, and ensure regulatory alignment with cGMP requirements for dietary supplements.

The role requires strong documentation, cross-functional collaboration, and ability to respond swiftly to inspection findings while maintaining audit records and continuous improvement initiatives.