The Quality Manager (Pharma/Medical Domain) is responsible for leading and optimizing quality management systems across regulated manufacturing environments. This role focuses on aligning stakeholders, evaluating current quality processes and systems, and defining practical, business-aligned capabilities to enhance quality operations. The position plays a key role in driving strategic improvements in areas such as CAPA, non-conformance, audits, supplier quality, and laboratory systems while ensuring compliance with regulatory standards. The Quality Manager will also develop a phased roadmap to modernize and streamline quality processes within the existing technology landscape.

• Align cross-functional stakeholders on priority quality use cases such as environmental monitoring, swab testing, non-conformance management, CAPA, audits, supplier quality, and LIMS.