Guerbet is seeking a QC LCM/Stability Lead to drive analytical method validation and stability programs in a cGMP setting in the United States. You will serve as SME during FDA/EMA inspections, lead method lifecycle management, and mentor junior staff to uphold data integrity and regulatory compliance.
Responsibilities include designing validation protocols, interpreting results, and guiding CAPA activities while collaborating with QA, Regulatory Affairs, Manufacturing, and R&D to support
#J-18808-LjbffrLead, Analytical Method Validation & Stability in nc at Unknown Company
This position is listed as full time and onsite.