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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