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BSP Pharmaceuticals S.p.A is a CDMO dedicated to development and manufacturing for cytotoxic and non-cytotoxic products. The QC Chemical Analyst will perform chemical analysis, operate HPLC/UPLC/U V instruments, and contribute to documentation and data integrity in a cGMP setting.
The role requires a Master's in Chemistry, 2+ years in a similar environment, GMP knowledge, and English working proficiency. Availability for shifts is essential to support multi-site operations.
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