Scarborough, ME30+ days ago
Draft validation protocols, execute validations, and draft validation reports for reagents manufacturing processes (i.e. mixing, pooling, cleaning) operational qualification (OQ), test method validation (TMV), performance qualification (PQ), and process validation (PV) are all within scope. " Develop and maintain data tracking sheets for experiment results, critical process parameter (CPP) operating ranges, critical quality attribute (CQA) results across manufacturing events.