Tris Pharma, Inc. in New Jersey seeks an APQR Program Lead to oversee annual product quality reviews, merge data evaluation with cGMP controls, and ensure products meet safety and quality standards.
The role involves leading trend analysis across CQAs and CPPs, driving CAPAs and investigations, and preparing reports for FDA inspections, with a focus on data-driven quality improvements and strong collaboration across QA, manufacturing, and labs.
#J-18808-LjbffrAPQR Program Lead - Quality & Process Analytics in jersey city at Unknown Company
This position is listed as full time and onsite.