GCP Process

3 settimane fa


siena, Italia Philogen A tempo pieno

A biotech company in Tuscany is seeking a Process & Computer System Validation Specialist (GCP) to validate and maintain computerized systems, ensuring compliance with GMP/GCP regulations. The ideal candidate has a technical/scientific degree and at least 2 years of experience in the pharmaceutical sector. Responsibilities include managing validation documentation and participating in audits. This role requires strong problem-solving skills and collaboration abilities.#J-18808-Ljbffr



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