Nutraceutical QA Auditor - Audit Lead & Vendor Compliance

Astrix

Charleston (SC)

On-site

USD 70,000 - 95,000

Full time

14 days+
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Job summary

Astrix in the Charlotte metro area is seeking a Quality Assurance Auditor to join our team. This role involves leading audit planning, internal and external audits, and ensuring compliance with cGMP and FDA regulations to support high-quality nutraceutical products.

The ideal candidate has a Bachelor's degree in a scientific field, 5 years of QA auditing experience in an FDA-regulated setting, and willingness to travel to supplier sites on short notice.

Qualifications

  • Bachelor’s degree in a scientific field.
  • 5 years of QA auditing experience in a cGMP environment & external vendor/supplier compliance within an FDA regulated industry.
  • Knowledge of Regulations 21 CFR Part 210, 211, 507 as the dietary supplements regulations 21 CFR.
  • Experience with internal & external auditing.

Responsibilities

  • Manage audit planning, scheduling, and execute internal and external audits.
  • Maintain the vendor qualification program including the Approved Vendor List and supplier corrective action request program (SCAR).
  • Manage external vendor(s) responsible for international audits.
  • Manage all documents relating to audits, vendors, and suppliers in a QMS.
  • Determine the level of risk of findings identified and follow up on corrective actions.
  • Develop and implement a performance tracking system and reporting of departmental compliance.
  • Train and assist internal departments to understand and comply with Quality and Compliance expectations.

Skills

Auditing
Vendor management
Regulatory knowledge
Travel readiness

Education

Bachelor's degree in a scientific field

Tools

QMS systems

Job description

Astrix in the Charlotte metro area is seeking a Quality Assurance Auditor to join our team. This role involves leading audit planning, internal and external audits, and ensuring compliance with cGMP and FDA regulations to support high-quality nutraceutical products.

The ideal candidate has a Bachelor's degree in a scientific field, 5 years of QA auditing experience in an FDA-regulated setting, and willingness to travel to supplier sites on short notice.

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