Executive-QA

At ALS, we encourage you to dream big. When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. 1. Review of Documents and Records: Review analysis records, MOA and SOPs to ensure compliance with GMP and regulatory requirements. Approval or rejection (as applicable) of procedures or specifications impacting the identity, strength, quality, and purity of the drug product/drug substance. Review of qualificat…