Senior Internal Audit QA Manager - GMP Compliance

FOCUS - A Cormica Lab; New Jersey; On-site; USD 110,000 - 150,000; Full time

Job summary

TPM Laboratories, Inc. in Cherry Hill, NJ seeks an Internal Audit QA Manager to provide independent oversight of quality and compliance systems, supporting cGMP adherence and inspection readiness. You will evaluate analytical data, validation work, and quality records, driving practical improvements.

The role requires senior QA experience, internal audit expertise, and strong leadership to guide cross-functional teams and coordinate with Sales and senior management during audits and inspections.

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 OOS/OOT, deviations, CAPA, and change controls; conduct trending and recommend actions.
• Confirm alignment to FDA, ICH, USP, 21 CFR 210/211, ALCOA+ and internal standards.
• Support client/regulatory audits and provide GMP guidance and training.
• Lead a team as section head, manage priorities/resources, and partner with Sales and senior leaders.

Skills

GMP/ISO 17025

Internal auditing

People leadership

Job description

TPM Laboratories, Inc. in Cherry Hill, NJ seeks an Internal Audit QA Manager to provide independent oversight of quality and compliance systems, supporting cGMP adherence and inspection readiness. You will evaluate analytical data, validation work, and quality records, driving practical improvements.

The role requires senior QA experience, internal audit expertise, and strong leadership to guide cross-functional teams and coordinate with Sales and senior management during audits and inspections.