Summary from listing
Guerbet is hiring a QC LCM/Stability Lead to provide technical leadership and oversight of analytical method validation and stability programs in a cGMP-regulated pharmaceutical environment. The role serves as a subject matter expert for regulatory inspections and audits, approves validation documentation, leads method lifecycle management and investigations, supports cross-functional product and regulatory activities, and mentors junior analysts and scientists. Candidates need a bachelor’s degree in chemistry or a related scientific field with 10+ years of experience, or a master’s degree with 5+ years, or a PhD with 2+ years, along with extensive analytical method validation experience.
