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Quality Assurance Manager of Internal Audits

Focus Laboratories


Job Location:

Cherry Hill, NJ - USA

Monthly Salary: Not provided by the employer
Posted: 29 September 2026 (Yesterday)
Application Deadline: 27 December 2026
Vacancies: 1 Vacancy

Job Summary

Who We Are

TPM Laboratories Inc. is an independent contract testing laboratory providing personalized analytical services to the pharmaceutical and chemical industries. TPM Labs specializes in Analytical Research and Development Testing Services Quality Control Testing and Stability Storage & Testing Services.

Our goal is to provide high quality cost effective and timely service personalized to meet your needs.

Role Summary

The Internal Audit QA Manager provides independent oversight of TPMs laboratory quality and compliance systems to support cGMP adherence and inspection readiness. You will evaluate analytical data validation work and quality records and identify compliance risk while driving practical continuous improvement.

Key responsibilities include:
- 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

Required qualifications/skills:
- 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

Apply if you can lead with integrity and keep quality decisions clear and defensible.

Daily Flow

Youll work onsite in Cherry Hill NJ MondayFriday 8:30am5:00pm balancing planned audit work with real-time quality decisions. The day typically includes focused time reviewing documentation and data in detail then short direct discussions with analysts and leaders to confirm facts and close gaps. Youll keep inspection readiness moving by tracking open items to completion and setting clear priorities for your team. When clients or auditors are on site (or requesting information) youll help coordinate responses and keep communication tight and professional. Youll also spend time aligning with Sales and senior management on upcoming work timelines and risk areas so quality oversight supports delivery without surprises.


Required Experience:

Manager


About Company

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FOCUS Laboratories provides microbiological testing and consultation services to the pharmaceutical, cosmetic, biotechnology, and medical device industries.

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