Resultados de la búsqueda: 2 vacantes
...and irregular hours)
Experience in:
QSR, GMP, ISO, applied statistics and failure mode analysis techniques.
FDA 21 CFR and global medical device regulations and standards is required (including but not limited to MDD, MDR Regulations, International standards ISO...
...safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
Responsibilities:
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