MedPharm is seeking a Quality Engineer II-III to design, implement, and maintain the Quality Management System across the manufacturing lifecycle, supporting process validation and deviations with root-cause investigations.
You will oversee CAPAs, batch release review, and audits for GMP, GLP, and clinical programs, collaborating with manufacturing, engineering, supply chain, and QA teams to drive continuous improvement.
#J-18808-LjbffrSenior Quality Engineer – GMP, Validation & CAPA in durham at Unknown Company
This position is listed as full time and onsite.