Qc Analyst
1 week ago
**Summary**:
Deze rol maakt gebruik van chemische laboratoriumvaardigheden om producten of materialen te testen en te meten, terwijl ervoor wordt gezorgd dat de analyse wordt uitgevoerd volgens vastgestelde standaard operationele procedures (SOP's), analytische methoden en de huidige Compendia.
**About the Role**:
Major Accountabilities
~ Monsteropslag en -beheer
~ Analytische testen/documentatie van geneesmiddel/ eindproduct / klachten / stabiliteit / verpakkingsmateriaal monsters volgens GxP-normen
~ Testen/Sample-opslag en -beheer.
~ Analytische documentatie van stabiliteitsmonsters volgens GxP-normen
~ Melding van technische klachten / bijwerkingen / scenario's voor speciale gevallen met betrekking tot Novartis-producten binnen 24 uur na ontvangst
~ Distributie van monsters voor het in de handel brengen (indien van toepassing)
Key Performance Indicators
Deze rol maakt gebruik van chemische laboratoriumvaardigheden om producten of materialen te testen en te meten, terwijl ervoor wordt gezorgd dat de analyse wordt uitgevoerd volgens vastgestelde standaard operationele procedures (SOPs), analytische methoden en de huidige Compendia.
Work Experience
~gedegen technische en wetenschappelijke kennis van farmaceutische/chemische analysen/QC/gelijkwaardig
~Werkervaring in een laboratoriumomgeving in de farmaceutische industrie
**Skills**:
~Laboratoriumapparatuur
~Kwaliteitscontrole (Qc) testen
~Kwaliteitscontrole Bemonstering
~Totaal kwaliteitsmanagement
~Gxp
~Industriestandaarden
~Uitmuntendheid in laboratoria
~Besluitvormingsvaardigheden
~Omgaan met ambiguïteit
~Zelfbewustzijn
~Continu leren
~Technologische expertise
Language
Engels
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
Regelmatig
Shift Work
No
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