QA Manager - GMP Compliance & Data Integrity

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

Job summary

TPM Laboratories, Inc. is seeking a QA Manager to lead the quality system and ensure cGMP compliance across documentation, investigations, and releases.

You will oversee QA staff, maintain policies and SOPs, approve methods and validation protocols, and drive continuous improvement through audits and CAPA.

The role emphasizes data integrity, inspection readiness, client and regulatory support, and training to elevate quality across all laboratory activities.

Qualifications

• Bachelor’s degree in Chemistry or related discipline.
• 6–8 years in a regulated pharmaceutical/laboratory environment.
• Strong QA systems, audit, and compliance oversight experience.
• Proven review/approval of scientific and regulatory documentation.
• People leadership experience; knowledge of ALCOA+ and 21 CFR 210/211.

Responsibilities

• Lead the quality system and ensure cGMP, FDA, ICH, USP, and internal requirements are met.
• Protect data integrity and keep site inspection-ready; provide QA governance across documentation, investigations, and releases.
• Oversee QA staff, policies, SOPs, and controlled documents; approve methods, specifications, and validation protocols.
• Review analytical data for accuracy and compliance; oversee OOS/OOT, deviations, CAPA, and change control; trending quality events.
• Support client and regulatory audits; drive GMP training and continuous improvement.

Skills

QA systems

Audit & compliance

Documentation review

People leadership

ALCOA+ & 21 CFR 210/211

Education

Bachelor’s in Chemistry

Job description

TPM Laboratories, Inc. is seeking a QA Manager to lead the quality system and ensure cGMP compliance across documentation, investigations, and releases.

You will oversee QA staff, maintain policies and SOPs, approve methods and validation protocols, and drive continuous improvement through audits and CAPA.

The role emphasizes data integrity, inspection readiness, client and regulatory support, and training to elevate quality across all laboratory activities.