Qc Analyst
1 week ago
**Summary**:
~ Diese Rolle nutzt chemische Laborfähigkeiten, um Produkte oder Materialien zu testen und zu messen und gleichzeitig sicherzustellen, dass die Analyse gemäß etablierten Standard Operating Procedures (SOPs), Analytischen Methoden und aktuellen Kompendien durchgeführt wird.
**About the Role**:
Major Accountabilities
~ Probenlagerung und -verwaltung
~ Analytische Prüfung/Dokumentation von Arzneimitteln/Fertigprodukten/Reklamationen/Stabilität/Verpackungsmaterialproben nach GxP-Standards
~ Testen/Beispielspeichern und -management.
~ Analytische Dokumentation von Stabilitätsproben nach GxP-Standards
~ Meldung von technischen Beschwerden / unerwünschten Ereignissen / Sonderfallszenarien im Zusammenhang mit Novartis-Produkten innerhalb von 24 Stunden nach Erhalt
~ Verteilung von Vermarktungsmustern (falls zutreffend)
Key Performance Indicators
~ Diese Rolle nutzt chemische Laborfähigkeiten, um Produkte oder Materialien zu testen und zu messen und gleichzeitig sicherzustellen, dass die Analyse gemäß etablierten Standard Operating Procedures (SOPs), Analytischen Methoden und aktuellen Kompendien durchgeführt wird.
Work Experience
~Fundierte technische und wissenschaftliche Kenntnisse der pharmazeutischen/ chemischen Analytik/QC/Äquivalentes
~Arbeitserfahrung in einer Laborumgebung in der pharmazeutischen Industrie
**Skills**:
~Laborausstattung
~Qualitätskontrolle (Qc) Prüfung
~Qualitätskontrolle Probenahme
~Umfassendes Qualitätsmanagement
~Gxp
~Industriestandards
~Exzellenz im Labor
~Fähigkeiten zur Entscheidungsfindung
~Umgang mit Mehrdeutigkeit
~Selbsterkenntnis
~Kontinuierliches Lernen
~Technologisches Know-how
Language
Englisch
Division
Operations
Business Unit
Universal Hierarchy Node
Location
Singapore
Site
Tuas South Avenue
Company / Legal Entity
SG12 (FCRS = SG012) Novartis Singapore Pharmaceutical Manufacturing Pte Ltd
Functional Area
Quality
Job Type
Full time
Employment Type
Regulär
Shift Work
No
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