Validation Supervisor - Pharmaceutical Company

💼 Azienda: Chaberton Professionals
📍 Luogo di Lavoro: Latina, Lazio, Italia
🕒 Data Annuncio: 06-05-2025

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Chaberton Professionals , a division of Chaberton Partners dedicated to the research and selection of Middle Management profiles, is currently looking for a Validation Supervisor for a pharmaceutical company.

The Supervisor, Validation will:

• Supervise and manage calibration and requalification teams to ensure efficient and accurate operations.
• Build and update calibration plans for GMP instruments, ensuring strong adherence to procedures.
• Coordinate requalification plans for GMP equipment, ensuring adherence to business and regulatory standards.
• Review and update calibration and requalification procedures in coordination with relevant functions.
• Ensure compliance with company quality standards and report any non-compliance.
• Manage the budget for the calibration and requalification activities.

Requirements:

• Technical or Scientific Degree (Mechanical Engineering, Chemical Engineering, CTF, Biomedical Engineering, Pharmacy, Industrial Chemistry) with proven experience in calibration and requalification activities in the pharmaceutical sector.
• Familiarity with pharmaceutical GMP, SOPs, and quality standards (at least 3 years) and ability to strictly adhere to procedures and safety regulations.
• Experience managing teams and coordinating with external service providers (at least 2 years).
• Outstanding organizational skills to manage multiple tasks and priorities; analytical abilities to review and interpret data efficiently.
• Good communication and leadership skills, as well as collaborative approach to effectively work with cross-functional teams.
• Fluent in English.

Location: Prov. Latina

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