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.
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Job Description
Major Accountabilities:
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QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones, Functional Breadth, Collaborating across boundaries
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Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
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Distribution of marketing samples (where applicable)
Key Performance Indicators:
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On-time and GMP-compliant release of dosage forms
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No complaints about inspections by authorities in your own area of responsibility without these being noticed & communicated beforehand
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Successfully support continuous improvement projects
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Executes batch release in compliance with registration
Work Experience:
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Quality Assurance
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Quality Control
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Quality Management Systems
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Technological Expertise
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Environmental Monitoring
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Release Management
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Good Manufacturing Practices (cGMP)
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Audit & Inspection Management
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Quality Compliance
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Technological Expertise
Skills:
Languages:
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Skills Desired
Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge