Visual Inspection Lead

Takeda Pharmaceutical

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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

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