Responsibilities Chemical analyses on incoming raw materials and finished products Deviation reporting and root cause investigation Data collection and analysis Control and recording of results in compliance with GMP procedures Collaboration on innovative projects aimed at improving and optimizing laboratory processes Requirements ~ Degree in Chemistry or Pharmaceutical Chemistry and Technology (CTF) ~2-3 years of experience as a QC laboratory analyst/technician within a pharmaceutical manufacturing environment ~ Autonomous use of HPLC instrumentation ~ Good command of English (B2 level) ~ Work on a 2-shift schedule
📌 Pharmaceutical Quality Control Analyst (Origgio)
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📍 Origgio
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