Manager, Global Stability

Relocation Assistance Offered Within Country Job Number #176318 - Piscataway, New Jersey, United States Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.   As the Manager, Global Stability, you will serve as the strategic leader and accountable owner of Colgate-Palmolive's global product stability program, sitting within the Global Quality organization. This high-impact role offers an exciting opportunity to drive regulatory compliance, technical excellence, and data integrity across all Manufacturing Sites and Global Technology Centers worldwide. Your primary mission will be to ensure robust compliance with global regulations and ICH guidelines while leading the continuous digital evolution of our stability data frameworks. Responsibilities: Define and execute the global stability strategy to guarantee continuous compliance with all applicable global regulations, ICH guidelines, and internal Quality Standards Oversee and approve stability protocols, studies, data, and technical documentation prepared for submission to external regulatory agencies Partner cross-functionally with key collaborators across the R&D community, Manufacturing Sites, and Global Technology Centers to provide technical guidance and troubleshoot global program issues Drive robust investigations into stability OOS/OOT results, ensuring rigorous root cause analysis, sound scientific conclusions, and effective CAPAs Lead the digital governance and global enhancement of LIMS stability modules and analytics dashboards to monitor compliance, program metrics, and chamber capacity Serve as the primary Subject Matter Expert (SME) during internal and external regulatory inspections, while leading the internal Stability Community of Practice to scale organizational knowledge Required Qualifications: Bachelor’s Degree in Engineering, Chemistry, or a related Biological Science field At least 8 years of experience in a cGMP regulated environment  Experience leading multi-category Stability programs and Quality Systems In depth technical knowledge of cGMP, FDA regulations, 21 CFR 210 & 211, and ICH guidelines Demonstrated project management experience managing regulatory documentation or data-driven technical programs Deep technical skills in validation concepts, statistical trend analysis, and quality-related systems such as LIMS, LabNet, and ETQ Preferred Qualifications: Master’s…