To manage all Quality Control Activities, such as environmental monitoring, microbiological lab, product in-process, final release testing, raw materials incoming QC and all related activities as process improvement technology transfers, sub-contracting and GMP conformity.To ensure that the Quality Control is compliant with current worldwide good manufacturing practices and regulatory requirements.To ensure a consistent customer focused analytical service to Aubonne site to guarantee the supply of quality products according to the established plan, good manufacturing practices, registration product files and site quality standards.To ensure the use of validated/qualified analytical methods, systems and equipments. To ensure reliable and accurate QC documentation.To ensure transfer of new analytical tests methods according to company needs.Provide analytical support to the development or transfer of production processes, including validation batches.To be the point of reference on site for all analytical activities, and projects. To program future instrument and Technology improvements.To manage the capital budget for the department and all QC projects within agreed financial limits, providing regular reports and forecasts. Who you are:Chemistry, biology or pharmacy university degree+10 years experience in biopharmaceuticals manufacturing in analytical, production or related fields / + 3 years experience in pharmaceutical analytics, Technology transfers, Project managementProven large teams managerial experience, demonstrated leader with good communication skills (minimum 5 years)Sound awareness of cGMP related aspects and health authorities requirements including experience in facing inspectors during inspections.To react and resolve all managerial, technical and financial issues in the department autonomously in a timely and positive manner.Innovative, Collaborative and Result drivenFluent in French and English