Visual Inspection Lead

3 settimane fa


Vicenza, Veneto, Italia Takeda Pharmaceutical A tempo pieno

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:

Objective: To oversee the activities and personnel of the Visual Inspection department in Pisa, ensuring that they are carried out in compliance with clear and defined operating procedures and quality criteria.

Key Responsibilities:

• Supervise and coordinate the activities within the Visual Inspection department, ensuring that they are executed in accordance with defined quality criteria and operating procedures.

• Ensure compliance with EHS regulations during working hours for the entire department.

• Ensure the achievement of production volume targets set by the Supply Chain, guaranteeing the compilation of the Production Program in accordance with established Plant targets defined in Budget and Forecast (MPS/LT Fulfilment).

• Coordinate the visual inspection of unlabeled product and Media Fill according to reference SOPs.

• Organize the qualification operations of VI personnel, coordinate training, and development plans 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.

• Meet business KPIs in terms of VI process timelines, communicate any delays, and adjust the VI production plan accordingly.

• Coordinate the activities of VI personnel to meet the production plan, conduct training, and evaluate the performance of subordinates.

Requirements:

• 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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