Senior C&Q Specialist - Pharma, GMP, Bilingual

A leading technical support firm based in Puerto Rico is seeking a skilled professional to support Commissioning and Qualification (C&Q) activities geared towards pharmaceutical manufacturing. Candidates should have over 5 years of experience in equipment validation and a strong understanding of cGMP regulations. Bilingual candidates fluent in English and Spanish are preferred. This role involves ensuring compliance, managing documentation, and facilitating knowledge transfer within teams to maintain high quality in operations.
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