Visual Inspection Lead

1 settimana fa

Pisa, Toscana, Italia Takeda A tempo pieno

About the Role

This is a challenging and rewarding opportunity to join Takeda as a Visual Inspection Lead, where you will play a critical role in ensuring the quality and integrity of our products. As a key member of our team, you will be responsible for supervising and coordinating the activities of the Visual Inspection team, ensuring that all processes are executed in compliance with established procedures and quality criteria.

Key Responsibilities

  • Supervise and coordinate the activities of the Visual Inspection team, ensuring that all processes are executed in compliance with established procedures and quality criteria.
  • Ensure compliance with EHS regulations and company policies during working hours.
  • Responsible for achieving production volume targets set by the Supply Chain.
  • Coordinate the visual inspection of unlabeled product and Media Fill according to reference SOPs.
  • Organize qualification operations of Visual Inspection personnel, coordinate training and development plans for direct and indirect reports.
  • Participate in managing review of procedures, training, activities related to opening and investigating events, validations, and Change Control in Visual Inspection.
  • Responsible for meeting business KPIs in terms of VI process timelines, communicating any delays, and adjusting the VI production plan accordingly.
  • Coordinate Visual Inspection personnel and plan their activities to meet production plan and conduct training; responsible for evaluating the performance of subordinates.
  • Responsible for interactions within the network and global programs related to Visual Inspection.
  • Guarantee 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.

Requirements

  • Bachelor's/Master's degree in Chemistry, Pharmaceutical Chemistry, Biology, or related field.
  • Knowledge of cGMP and 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.

What We Offer

Takeda is a global pharmaceutical company committed to bringing better health and a brighter future to people worldwide. We offer a dynamic and supportive work environment, competitive compensation and benefits, and opportunities for professional growth and development.

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