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Job DescriptionJob Title: R0126792 Visual Inspection Lead
Location: Pisa
ABOUT THE ROLE: As a Visual Inspection Lead, you will oversee and manage activities within your scope, coordinating and controlling these through the guidance of VI Shift leaders.
You ensure that all tasks are carried out in strict adherence to clearly defined operating procedures, guaranteeing that processes and products meet established quality standards.
Additionally, you are responsible for ensuring compliance with EHS regulations throughout your working hours across the entire department.
Lastly, you are accountable for achieving the production volume targets set by the Supply Chain.
HOW YOU CONTRIBUTE: Guarantee compilation of the Production Program in accordance with the previously established Plant targets defined in Budget and Forecast (MPS/LT Fulfilment).Coordinate the visual inspection of unlabelled product and Media Fill according to the reference SOPs.Organize the qualification operations of the VI personnel.
Coordinate training and development plan of direct and indirect reports.Participate in managing the review of procedures, training, activities related to opening and investigating events, validations, and Change Control in visual inspection.Be responsible for meeting the business KPI in terms of VI process timelines, communicating any delays, and adjusting the VI production plan accordingly.Coordinate the VI personnel and plan their activities to meet the production plan and conduct training; be responsible for evaluating the performance of their subordinates.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 relevant years in the pharmaceutical field.Knowledge of the visual inspection process of Albumin.Knowledge of Visual Inspection regulations.Knowledge of MBRs and SOPs in the VI department.Communication, Influential and presentation skills.Digital/innovation oriented.Good knowledge of the English language.More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do.
We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine: Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
LocationsWorker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
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