Kindeva Drug Delivery in Missouri seeks a seasoned QA Validation SME to lead our validation function at a sterile injectable GMP site. You will guide equipment and utility qualification, process validation, media fills, CSV, and data integrity, ensuring regulatory alignment and robust quality systems.
You will collaborate with Engineering, Validation, Manufacturing, IT and QC, mentor staff, and serve as SME during inspections by FDA/EMA.
#J-18808-LjbffrSenior QA Validation Lead – Sterile Manufacturing in mo at Unknown Company
This position is listed as full time and onsite.