Qa Associate

Resource will cover volume driven operational activities in Novartis Country Quality (NCQ) for the whole Region Europe – deviations, escalations, supplier qualification support, etc.
Local releases currently are out of scope, as country requiring such local releases (legal requirements) will have resources locally for that local releases.
To contribute to prevent significant quality issues or regulatory non-compliance in RE NCQ countries, which could lead to product stock-out, withdrawal or which would negatively impact the quality of the products in scope (RLT).
To contribute to maintain cross-divisional standardization and efficiency gains through innovation and operational excellence projects within the product QA framework.
About the RoleMajor accountabilities: Contribute to ensure proper scheduling and prioritization of the QA RLT products related activities in RE NCQ in alignment with relevant business stakeholders.Ensure strong collaboration, partnering and networking with EU stakeholders and other QA Regional / Global key representatives.Become a key business partner with all business process owners.Key performance indicators: Performance against Key Quality Indicators.Work Experience: Operations Management and Execution.Skills: Change Control.Dealing With Ambiguity.Guideline.Product Release.QA (Quality Assurance).Quality Management.Regulation.Technological Expertise.Languages: Master Degree in Pharmacy or similar.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
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Functional Area: Quality
Job Type: Full time
Employment Type: Regular
Shift Work: No
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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