Quality Assurance

- Ensures full QA support and supervision of QA related activities
- Ensures that the various operations in local organization are associated with gobal quality system
- Internal process set up, Quality system implementation, audit and self-inspection
- Reporting about all deficiencies or observations to global QA
- Ensures that all aspects of the handling and distribution of pharmaceutical products at the site/in the country and all other QA related activities comply with the requirements of the Novartis Quality Manuals (QM), Sandoz GOPs and internal company SOPs
- Ensures that Quality System and all Standard Operating procedures (SOPs) are in place for all GXP related activities and that compliance is maintained through training and internal audits
- Ensures co-ordination between all stakeholders (3rd parties, CO SK, Quality organisation of Sandoz…)
- Coordinates all activities related to repackaging
- Ensures that all activities related to »complaints«, »recalls« are performed in accordance with the relevant QM and are in compliance with the local regulations and Sandoz standards
- Reports to Head of Medical & Regulatory

- Práca v medzinárodnej spoločnosti
- Odborné školenia
- Príjemné pracovné prostredie
- Služobný mobilný telefón a laptop

Ak vás daná ponuka zaujala a spĺňate požadované kritériá, zašlite, prosím vaše CV na adresu: [email protected] v termíne do 14. 10. 2014. Do predmetu správy uveďte "QA".
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