Teamlead Deviation and GMP Support

Key responsibilities:

· Being responsible for staffing, training and development through continuous learning to retain energized, motivated and team oriented staffs

· Utilize and allocate the resources of the team in an efficient and effective manner through cross training/ flexible resource planning

· Work with Stakeholders to ensure cGMP compliance in all aspects of the GMP deliverables under its accountability

· Collaborate with stakeholders and SMEs e.g Ops BPEs, MSAT group, Engineering, QC to bring about process robustness/ improvements to routine manufacturing via CAPA strength

· Responsible for meeting deviations timelines in order to meet production and batch release schedules while ensuring appropriate level of investigation quality · Along with the Ops Managers, set and ensure alignment and consistency from technical and quality prospective in the different ops departments

· Help develop and manage information systems to monitor the efficiency and success of the implemented CAPAs and CRs

Key requirements:

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference .