Quality Assurance Manager (JMR)
Job Location: Randolph, NJ
Date Posted: 2021-05-12
Growing Pharmaceutical company needs someone to lead a group to ensure compliance with GMP, FDA regulations, review and approve quality system documentation including SOPs, batch records, and provide support for the manufacturing of aseptic drug products in a clean room environment. Will perform root cause analysis and implement corrective actions as well as assist with supplier qualifications and internal/external audits. Position will require 5+ years in QA Management with aseptic/parenteral manufacturing/development experience and validation of aseptic drug product manufacturing preferred. Travel will be 10%.
Please contact Joe Raia at email@example.com
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