Quality Assurance Manager

ACE Partners; Pohatcong Township (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

ACE Partners is seeking a QA Manager for its site in Pohatcong, NJ. This hands-on leadership role oversees QA operations in an FDA-regulated manufacturing environment.

Responsibilities include leading the QA team, directing CAPA/NCR, auditing QMS, and ensuring cGMP compliance while aligning with FDA, IPEC, and ISO requirements.

Qualifications

• Bachelor's degree in a life science discipline (or equivalent experience).
• 5+ years of progressive Quality Systems experience in a regulated manufacturing environment.
• Strong working knowledge of FDA and international quality regulations.
• Supervisory experience preferred.

Responsibilities

• Lead, train, and develop the Quality Assurance team.
• Direct the CAPA/NCR program and lead complaint investigations and root cause analysis.
• Conduct internal QMS audits and maintain cGMP compliance.
• Ensure alignment with FDA, IPEC, and ISO requirements.
• Partner with customers, suppliers, and production leaders on quality requirements, supplier performance, and corrective actions.
• Provide strategic quality insight to senior management and drive continuous improvement.

Skills

Leadership

Communication

Problem solving

Team development

Education

Bachelor's degree in life science

Job description

QA Manager

Pohatcong, NJ

$110,000 - $150,000

ACE Partners is working with a leading life sciences manufacturer to hire a Quality Assurance Manager at their site in New Jersey. This is a hands-on leadership role overseeing QA operations in an FDA-regulated manufacturing environment.

What you'll do:

• Lead, train, and develop the Quality Assurance team
• Direct the CAPA/NCR program and lead complaint investigations and root cause analysis
• Conduct internal QMS audits and maintain cGMP compliance
• Ensure alignment with FDA, IPEC, and ISO requirements
• Partner with customers, suppliers, and production leaders on quality requirements, supplier performance, and corrective actions
• Provide strategic quality insight to senior management and drive continuous improvement

What we're looking for:

• Bachelor's degree in a life science discipline (or equivalent experience)
• 5+ years of progressive Quality Systems experience in a regulated manufacturing environment
• Strong working knowledge of FDA and international quality regulations
• Supervisory experience preferredExcellent communication, organizational, and leadership skills