Summary
About the Role
Major accountabilities:
- Contribute to ensure proper scheduling and prioritization of the QA RLT products related activities 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:
EU stakeholder satisfaction
Performance against Key Quality Indicators.
Minimum Requirements:
Work Experience:
- Master Degree in Pharmacy or similar
- Fluent written/spoken English
- At least 5 years in Quality Assurance area in Pharmaceutical Companies
- QA background (plus: nuclear know how) with international exposure
Skills:
- Continuous Learning.
- Dealing With Ambiguity.
- Decision Making Skills.
- Gxp.
- Industry Standards.
- Laboratory Equipment.
- Laboratory Excellence.
- Managing Resources.
- Organizational Savvy.
- Quality Control (Qc) Testing.
- Quality Control Sampling.
- Self Awareness.
- Smart Risk Taking.
- Technological Expertise.
- Total Quality Management.
Languages :
- English.
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? https://www.novartis.com/about/strategy/people-and-culture
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