Performing stability, validation, raw materials, packaging materials, semi-finished and finished products analyses
Conducting both manual and automated analyses
Calibrating and adjusting laboratory equipment
Preparing and storing reagents in accordance with established procedures
Following the analysis schedule and comparing results against current standards
Identifying anomalies and contributing to their resolution
Recording and verifying results, and issuing analysis reports
Proposing improvements in equipment organization
Ensuring maintenance of workstations and providing technical training to new team members

Bachelor’s degree (Bac+3/4) in Chemistry, Pharmaceutical Quality Control/Analysis, or equivalent
Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices)
Familiarity with laboratory equipment and IT systems
Ability to write procedures and reports
Strong organizational skills and attention to detail

Analyst, QC

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