Manages and coordinates daily duties and provide opportunities for training and development of the Quality Assurance (QA) Specialists. Monitor and maintain compliance with current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR), Points to Consider (PTC), International Conference on Harmonisation (ICH), Good Laboratory Practices (GLP), Good Tissue Practices (GTP) and relevant foreign regulatory guidelines for biopharmaceuticals. Drive continuous quality improvement through communication/training, waste reduction, and mistake-proofing. Solicit and implement industry best practices.
We are an Equal Opportunity Employer. Minorities/Women/Veterans/Disabled.