Senior Quality Compliance Auditor – Multi-Site & CAPA Lead

International Vitamin Corporation; Anderson (IN); On-site; USD 85,000 - 120,000; Full time

Job summary

International Vitamin Corporation in Anderson, IN is seeking a Sr. Quality Compliance Specialist to lead internal and external audits across multiple sites. You will manage CAPAs, document control, and regulatory submissions, ensuring cGMP compliance for dietary supplements.

The role requires a Bachelor’s in a quality-related field and 3–5 years of QA experience in dietary supplement or pharmaceutical manufacturing, with strong knowledge of FDA 21 CFR Part 111 and CAPA processes.

Qualifications

• Bachelor’s degree in Quality, Food Science, Biology, Chemistry, or a related discipline.
• 3–5 years of experience in Quality Assurance within dietary supplement or pharmaceutical manufacturing.
• Demonstrated experience conducting or coordinating internal and external audits.
• Strong working knowledge of FDA 21 CFR Part 111; familiarity with HACCP/FSMA is a plus.

Responsibilities

• Develop, implement, and maintain internal audit program across four sites; manage annual audit schedule.
• Lead audit teams, document findings, and track closure per CAPA requirements.
• Coordinate external audits, including planning, logistics, and on-site activities.
• Initiate and manage deviations, nonconformances, and CAPAs with root cause analysis.
• Draft and revise SOPs, work instructions, and quality records to ensure compliance.

Skills

Audit coordination

CAPA management

Documentation

Regulatory knowledge

Quality assurance

Written communication

Education

Bachelor’s degree in Quality

Tools

Electronic QMS

Job description

International Vitamin Corporation in Anderson, IN is seeking a Sr. Quality Compliance Specialist to lead internal and external audits across multiple sites. You will manage CAPAs, document control, and regulatory submissions, ensuring cGMP compliance for dietary supplements.

The role requires a Bachelor’s in a quality-related field and 3–5 years of QA experience in dietary supplement or pharmaceutical manufacturing, with strong knowledge of FDA 21 CFR Part 111 and CAPA processes.