The role is managing processes and tools, operations and activities enabling Quality Supply Chain and Compliance at a global level. The responsible person execute global quality compliance and supply chain activities deriving from the implementation of global supply chain projects and compliance expectations from Health Authorities. The role supports the supply of materials and services to Lonza within area of responsibility by assessing the quality of the Suppliers and their ability to meet defined requirements utilizing tools such as Quality Risk Management (QRM), supplier assessment/audit, change management, and complaint/deviation trend management.

Key responsibilities:

• Support in managing QAA templates and to complete / revise QAA and SCL in due time, route for review before initiating approval process. Interact with the suppliers and the sites to complete this activity
• Support role in assigned supply chain projects
• Support in performing of KPI monitoring
• Support supplier lifecycle: onboarding, monitoring and decommissioning
• Support in administrative activities related to DMS
• Support in creation and revision of SOP`s.

• Master or bachelor of Science in natural sciences (e.g. Biochemistry, Chemistry, Pharmacy, Microbiology, Biotechnology or equivalent)
• Previous experience in supply chain quality, material management and supplier quality management of the pharmaceutical industry is desired
• Previous knowledge in cGMPs and cGDP requirements and understanding of the regulatory process and requirements is desired
• Excellent English skills, both written and spoken.