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