About this opportunity
Avet Pharmaceutical lists this QA Director: Regulatory Compliance & cGMP Leadership opportunity in east brunswick township, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Avet Pharmaceutical seeks a Director of Quality Assurance to lead and optimize the cGMP program, audits, and regulatory readiness at the East Brunswick site.
The role directs QA systems, CAPA, batch disposition, deviations, investigations, and supplier qualification while partnering with Manufacturing, R&D, Engineering, Regulatory Affairs and other functions to ensure compliant products and processes.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.