By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. 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