Quality Auditor - On-Site GMP & Compliance (Mesa)

iS CLINICAL; Mesa (AZ); On-site; USD 30,000 - 33,000; Full time

Benefits offered by this job

401k

Life

Dental

Vision

Health

PTO

Job summary

Innovative Skincare in Mesa, AZ is hiring a Quality Auditor to perform audits of production, warehouse and quality processes on-site at our new Mesa facility. The role supports GMP compliance, CAPA verification, and continuous improvement by reviewing documentation, batch records, and reports for accuracy and conformance.

The candidate will train staff on quality standards, assist regulatory inspections, and help maintain audit records while working with QA, QC and Production teams.

Qualifications

• High school diploma or GED required; associate’s or bachelor’s degree preferred.
• 1–3 years of experience in quality assurance, auditing, or manufacturing preferred.
• GMP, SOPs, and regulatory standards knowledge required.
• Strong attention to detail and documentation accuracy.
• Good communication and problem-solving skills.
• Ability to work independently and with cross-functional teams.
• Stand/walk 8–10 hours during audits and inspections; wear PPE as required.

Responsibilities

• Conduct internal audits of production, warehouse, and quality processes.
• Review documentation, batch records, and reports for accuracy and compliance.
• Inspect finished products and packaging to verify quality standards.
• Identify and report non-conformances or deviations.
• Work with QA, QC, and Production teams to correct and prevent issues.
• Maintain audit records and assist in training on quality standards.

Skills

Attention to detail

Quality auditing

Documentation accuracy

GMP knowledge

Cross-functional teamwork

Independent work

Problem-solving

Communication

Physical stamina

PPE compliance

Education

High school diploma or GED

Associate’s or bachelor’s degree preferred

Job description

Innovative Skincare in Mesa, AZ is hiring a Quality Auditor to perform audits of production, warehouse and quality processes on-site at our new Mesa facility. The role supports GMP compliance, CAPA verification, and continuous improvement by reviewing documentation, batch records, and reports for accuracy and conformance.

The candidate will train staff on quality standards, assist regulatory inspections, and help maintain audit records while working with QA, QC and Production teams.