CT19 is seeking a Senior Quality Assurance Engineer to lead commissioning, qualification, and validation for a first-of-a-kind nuclear medicine production facility. You will own Master Validation Plan activities, oversee C&Q across equipment, utilities and processes, and drive validation reports in a highly regulated environment.
Ideal candidates have 5+ years in QA/validation within cgmp pharma manufacturing, deep knowledge of 21 CFR and cGMP, and experience with C&Q programs.
#J-18808-LjbffrSenior QA Engineer - cGMP Validation in Nuclear Medicine in wi at Unknown Company
This position is listed as full time and onsite.