Global Quality Program Integration Manager

Role: Manage global quality laboratory transformation initiatives within a biopharmaceutical manufacturing context, overseeing project integration, stakeholder collaboration, and budget management. Responsibilities: coordinate cross-functional teams regionally and globally, resolve conflicts, facilitate meetings, and ensure effective communication and operational excellence across projects. Lead process improvements and support business initiatives involving multiple internal and external stakeholders. Requirements: Bachelor's degree, 8+ years in pharmaceutical manufacturing or quality environment with regulatory compliance expertise, and 5+ years of project management experience. Strong communication, influencing, and stakeholder management skills are essential. High-Value: experience with FDA/EMA regulatory requirements, laboratory systems (LIMS/ELN), and managing complex, multi-stakeholder projects in a GMP/GLP setting. Work Setup: hybrid, with approximately 10% travel.