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Quality Control Technician

Novartis ACC · Ivrée

Nouveau
🇬🇧 English
cGMP GxP Microbiological verification Environmental monitoring

Description du poste

About the role

The Quality Control Technician ensures that finished products and incoming materials meet strict cGMP and SOP standards. Working in a regulated pharmaceutical environment, you will support both routine and specialized QC activities across rotating shifts, including night turns.

Key responsibilities

  • Perform batch analysis and raw material testing following specific training.
  • Conduct routine maintenance, cleaning, and microbiological verification of QC equipment.
  • Execute calibration, verification, qualification, and validation of QC processes and instruments.
  • Carry out QC sampling, environmental monitoring, and sterility testing, and report results.
  • Escalate and manage non‑conformances, deviations, OOS/OOT/OOE investigations, CAPA follow‑up, and change control activities.
  • Prepare analytical batch records, forms, and documentation in accordance with Good Documentation Practices.
  • Support internal and external audits and inspections.

Required profile

  • Degree in chemistry, biology or a related scientific field (preferred).
  • Experience in radiopharmaceutical or pharmaceutical QC environments is desirable.
  • Fluent in Italian and good command of English.
  • Willingness to work rotating shifts, including nights.

Required skills

  • cGMP compliance
  • SOP adherence
  • GxP knowledge
  • Microbiological verification techniques
  • Calibration of analytical equipment
  • Process validation
  • Environmental monitoring
  • Sterility testing

What we offer

  • Competitive benefits and rewards package.
  • Commitment to diversity, inclusion, and professional development.

Questions fréquentes

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Ivrée