The Validation Supervisor 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.
The company offers competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Location : Lazio