Specialist kontrole kakovosti II (m/f/d)
$27,510–$51,090 year
HybridMengeš, Mengeš, Slovenia
Job Summary
Conduct routine testing of elemental impurities, heavy metals, and nitrosamines in raw materials, intermediates, and finished products. Review, verify, and approve analytical results while preparing analytical documentation and interpreting data against regulatory requirements. Plan, execute, and document method validations, transfers, and optimizations; author validation reports and perform statistical analyses. Collaborate on investigations of analytical deviations, complaints, and corrective/preventive actions to ensure laboratory compliance with GMP and data integrity standards. Actively participate in inspections, internal audits, and continuous improvement projects while supporting colleagues and performing critical analyses as needed.
Required Qualifications
- Visokošolska stopnja izobrazbe farmacevtske, kemijske ali druge ustrezne naravoslovne smeri
- Natančnost, doslednost in visoka stopnja strokovne integritete pri delu
- Sposobnost sledenja navodilom, postopkom in zahtevam kakovostnega sistema
- Dobre komunikacijske veščine ter sposobnost učinkovitega sodelovanja z različnimi deležniki
- Aktivno znanje angleškega jezika
- Poznavanje orodij Microsoft Office
- Delovne izkušnje s področja kakovosti, razvoja, proizvodnje ali drugega reguliranega okolja
- Poznavanje dobre proizvodne prakse (GMP)
- Relocation Support: This role is based in Mengeš, Slovenija. Novartis is unable to offer relocation support: please only apply if accessible.
Desired Qualifications
- Delovne izkušnje s področja kakovosti, razvoja, proizvodnje ali drugega reguliranega okolja
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