GMP QA Officer: Shift-Based in Sterile Production

A leading pharmaceutical company based in Italy is seeking a QA Officer to ensure quality oversight over GMP activities in the production facility. Responsibilities include contributing to the validation of the production site, reviewing batch records, and supporting audits. Candidates should have a scientific degree, experience in a sterile production environment, and a good knowledge of GMP. Shift work, including nights and weekends, is a requirement. Fluency in Italian and good English are essential.
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