GMP Quality Audit Lead — Senior QA & Compliance

Focus Laboratories; Cherry Hill Township (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

TPM Laboratories, Inc. in Cherry Hill, NJ, is seeking an Internal Audit QA Manager to provide independent oversight of laboratory quality systems supporting cGMP adherence and inspection readiness.

You will evaluate analytical data, validation work, and quality records, and identify compliance risk while driving practical improvements. Key duties include performing audits, reviewing data packages, guiding CAPA and change controls, and ensuring alignment with FDA/ICH/USP and internal standards.

Qualifications

• Senior QA/compliance experience in a regulated lab environment (GMP/ISO 17025 or similar).
• Internal audit expertise; strong technical writing/review skills.
• People leadership, cross-functional communication, and sound judgment.

Responsibilities

• Perform internal audits and independent QA reviews of protocols, reports, and controlled records.
• Review/approve analytical data packages and data-release readiness.
• Assess deviations, CAPA, OOS/OOT, and change controls; conduct trending and recommend actions.
• Lead a team as section head, manage priorities/resources, and coordinate with Sales and senior leaders.

Skills

Senior QA/compliance experience

Internal audit expertise

People leadership

Cross-functional communication

Job description

TPM Laboratories, Inc. in Cherry Hill, NJ, is seeking an Internal Audit QA Manager to provide independent oversight of laboratory quality systems supporting cGMP adherence and inspection readiness.

You will evaluate analytical data, validation work, and quality records, and identify compliance risk while driving practical improvements. Key duties include performing audits, reviewing data packages, guiding CAPA and change controls, and ensuring alignment with FDA/ICH/USP and internal standards.