Descrizione Lavoro
A life sciences company in Italy is seeking a skilled CQV professional to plan and execute commissioning activities. The ideal candidate should have 2-3 years of technical experience, strong knowledge of FDA, GMP, and GAMP regulations, and excellent troubleshooting skills. Responsibilities include developing qualification protocols and maintaining detailed documentation. Good English language skills are required. This role is an excellent opportunity to work in a dynamic environment that values precision and adherence to industry standards.
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