On-Site Quality Auditor - GMP & CAPA Expert (Mesa, AZ)

iS CLINICAL

Mesa (AZ)

On-site

USD 30,000 - 33,000

Full time

14 days+
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Benefits offered by this job

401k
Life insurance
Dental
Vision
Health insurance
Paid time off

Job summary

Innovative Skincare, the home of the iS CLINICAL cosmeceutical brand, is seeking a Quality Auditor for our Mesa, AZ facility. The role audits processes, documentation, and finished products to ensure GMP compliance and regulatory standards.

The position is on-site with salary in a $22.00–$24.00 per hour range, depending on experience. Responsibilities include reviewing batch records, identifying non-conformances, supporting CAPAs, and assisting in regulatory inspections.

Qualifications

  • High school diploma required; higher education preferred.
  • 1–3 years in quality assurance, auditing, or manufacturing.
  • Knowledge of GMP, SOPs, and regulatory standards.

Responsibilities

  • Conduct internal audits of production, warehouse, and quality processes.
  • Review batch records, documentation, and reports for accuracy.
  • Inspect finished products and packaging for quality compliance.
  • Identify non-conformances and report deviations.
  • Collaborate with QA/QC/Production to correct issues.
  • Maintain audit records and assist in CAPA actions.
  • Train staff on quality and compliance standards.
  • Support inspections and customer audits; follow SOPs and safety rules.
  • Develop and follow audit schedules; observe practice for compliance.
  • Prepare written reports with findings, risks, and recommendations.
  • Track open findings until resolution.

Skills

Quality Auditing
Documentation Accuracy
GMP SOP Knowledge
Attention to Detail
Communication Skills
Independent Work
Cross-functional

Education

High school diploma
Associate or Bachelor’s preferred

Job description

Innovative Skincare, the home of the iS CLINICAL cosmeceutical brand, is seeking a Quality Auditor for our Mesa, AZ facility. The role audits processes, documentation, and finished products to ensure GMP compliance and regulatory standards.

The position is on-site with salary in a $22.00–$24.00 per hour range, depending on experience. Responsibilities include reviewing batch records, identifying non-conformances, supporting CAPAs, and assisting in regulatory inspections.

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