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 method validation reports. Plan, execute, and document method validations, transfers, and optimizations. Interpret statistical data and collaborate on investigations of analytical deviations, complaints, and corrective/preventive actions. Ensure laboratory activities comply with regulatory requirements, good manufacturing practices, and data integrity standards. Participate in inspections, internal audits, and continuous quality improvement projects. Share expertise with team members and perform critical analyses when business needs arise.
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
- Z izbranim kandidatom bomo sklenili delovno razmerje za določen čas enega leta s poskusno dobo 6 mesecev in z možnostjo dolgoročnega sodelovanja
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