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
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📌 Quality Control Analyst (Origgio)
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📍 Origgio
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