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Job Description 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 Locations ITA - Pisa Worker Type Employee Worker Sub-Type Regular Time Type Full time
