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Quality Control Technician

Novartis ACC · Ivrée

New
🇬🇧 English
cGMP SOP GxP microbiological verification calibration validation

Job description

About the role

The Quality Control Technician ensures that finished products and incoming materials meet strict quality standards in a cGMP environment. Working on rotating shifts, including night turns, you will support the laboratory and manufacturing teams to maintain compliance with Novartis quality standards.

Key responsibilities

  • Perform analytical testing of batches, raw materials, and finished products according to SOPs and cGMP rules.
  • Conduct routine maintenance, cleaning, and microbiological verification of QC equipment and pharmaceutical areas.
  • Execute calibration, verification, qualification, and validation activities for QC processes and instruments.
  • Support deviation investigations, OOS/OOT/OOE analyses, CAPA follow‑up, and change control management.
  • Prepare analytical batch records, maintain Good Documentation Practices, and report results.
  • Assist with internal and external audits, inspections, and qualification/validation projects.

Required profile

  • Degree in chemistry, biology or a related scientific field (preferred).
  • Experience in a radiopharmaceutical or pharmaceutical environment is desirable.
  • Fluent in Italian and good knowledge of English.
  • Ability to work rotating shifts, including night turns.

Required skills

  • cGMP compliance
  • SOP adherence
  • GxP knowledge
  • Microbiological verification
  • Calibration and validation of analytical equipment
  • Analytical testing and batch record documentation

What we offer

  • Opportunity to work for a global leader in medicines.
  • Access to Novartis benefits and development programs.
  • Inclusive and diverse work environment.

Questions fréquentes

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Published 2 giorni fa

Expires tra 1 mese

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Novartis ACC

Ivrée