Descripción del puesto:
Job Description Summary-Manages Quality aspects and projects within area of responsibility.
-Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.
Job Description
Major Accountabilities:
* QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones, Functional Breadth, Collaborating across boundaries
* Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
* Distribution of marketing samples (where applicable)
Key Performance Indicators:
* On-time and GMP-compliant release of dosage forms
* No complaints about inspections by authorities in your own area of responsibility without these being noticed & communicated beforehand
* Successfully support continuous improvement projects
* Executes batch release in compliance with registration
Work Experience:
* Quality Assurance
* Quality Control
* Quality Management Systems
* Technological Expertise
* Environmental Monitoring
* Release Management
* Good Manufacturing Practices (cGMP)
* Audit & Inspection Management
* Quality Compliance
* Technological Expertise
Skills:
* Collaboration
* Dealing With Ambiguity
* Operational Excellence
* Regulatory requirements knowledge
* Problem Solving Skills
* Leadership
* Communication skills
* Data Integrity
* Digital saviness
Languages:
* English.
Skills DesiredCollaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge
| Origen: | Web de la compañía |
| Publicado: | 17 Mar 2026 (comprobado el 18 Mar 2026) |
| Tipo de oferta: | Empleo |
| Idiomas: | Inglés |
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