Descripción de la oferta
PQE Group in Barcelona is seeking an experienced Commissioning, Qualification & Validation (CQV) Lead to drive equipment and system qualification in biotechnological production facilities. You will execute CQV activities, prepare and review URS, DQ, IQ, OQ, PQ protocols, and collaborate with Engineering, QA, Validation and Manufacturing to meet GMP, FDA, EMA, and ICH requirements.Fluency in Spanish and English is required, with a strong track record in regulated environments.
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