Visual Inspection Lead, Pisa Pisa

Visual Inspection Lead, Pisa
Pisa
Toscana, Pisa

OBJECTIVES/PURPOSE: • Supervises and knows the activities within their competence, which they coordinate and control through the guidance of the VI Shift leaders. • Ensures that the activities are carried out in compliance with clear and defined operating procedures to ensure that the process/product is executed/manufactured according to equally defined quality criteria. • Ensures compliance with EHS regulations during their working hours for the entire department. • Is responsible for ensuring the achievement of the production volume targets set by the Supply Chain. ACCOUNTABILITIES: • Guarantee compilation of the Production Program in accordance to the previously established Plant targets defined in Budget and Forecast (MPS/LT Fulfilment). • Coordinates the visual inspection of unlabeled product and Media Fill according to the reference SOPs. • Organizes the qualification operations of the VI personnel. Coordinates training and development plan of direct and indirect reports. • Participates in managing the review of procedures, training, activities related to opening and investigating events, validations, and Change Control in visual inspection. • Is responsible for meeting the business KPI in terms of VI process timelines, communicating any delays, and adjusting the VI production plan accordingly. • Coordinates the VI personnel and plans their activities to meet the production plan and conduct training; is responsible for evaluating the performance of their subordinates. • Is responsible for interactions within the network and global programs related to Visual Inspection. • Guarantee the respect of preventive/corrective maintenance operations, validation, and calibration activities on production equipment related to Crude Fractionation area. • Ensure that Visual Inspection personnel correctly complete production batch records and generally all Visual Inspection related documentation is correctly and timely prepared. WHAT YOU BRING TO TAKEDA: • Bachelor's/Master's degree in Chemistry, Pharmaceutical Chemistry, Biology, or related field. • Knowledge of cGMP. Previous experience in Team Management and at least 5 years in the pharmaceutical field. • Knowledge of the visual inspection process of Albumin. • Knowledge of Visual Inspection regulations. • Ability to interpret and modify the production program. • Knowledge of MBRs and SOPs in the VI department. • Knowledge of key leadership behaviors. • Communication, Influential and presentation skills. • Digital/innovation oriented. • Good knowledge of the English language. J-18808-Ljbffr