Novartis AG
Basel (City)
Expert Drug Supply
- 10 June 2026
- 100%
- Basel (City)
About the job
Summary
~This is a universal job description intended to capture some of the primary tasks of this role that are common to all functions or divisions. It is not intended to represent all specific responsibilities of the position ~ Organises, coordinates, monitors and executes activities related to the assigned area of responsibility. Ensures process compliance with multinational regulations, as well as Novartis internal procedures and GxP requirements.
About the Role
Major Accountabilities
~ Cooperation and collaboration with internal and external stakeholders (customers and/or suppliers, subject to liability conditions)
~ Contribute as a unit representative in project teams
~ Ensure deliveries are made.
~ Part-time members, such as
~ Inform your partner or customer of the issue.
~ Ensure knowledge is acquired in relevant procedures. (Troubleshooting is available)
~ Technical orientation and training as a technical expert or cook. As a mentor for beginners and senior colleagues.
~ Identify and implement resource constraints and cost reduction functionalities
~ Demonstrate a positive work ethic and influence others
~ Ideas for designing and applying processes for continuous improvement when you are a professional/organisational team or a senior member.
~ Ensure compliance with Novartis and other relevant regulations
~ Consolidate results to enable data evaluation and draw conclusions
~ Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
~ Distribution of marketing samples (if applicable)
Key Performance Indicators
~This is a universal job description intended to capture some of the primary tasks of this role that are common to all functions or divisions. It is not intended to represent all specific responsibilities of the position ~ Organises, coordinates, monitors and executes activities related to the assigned area of responsibility. Ensures process compliance with multinational regulations, as well as Novartis internal procedures and GxP requirements.
Work Experience
~Professional experience (approximately 3-5 years) in a GMP and analytical environment (e.g. quality control)
Skills
~Material Requirements Planning (MRP)
~Material management
~Project management
~Supply chain planning
~Supply chain management
~Master data
~WMS (Warehouse Management Systems)
~Production planning
~Continuous improvement process
Language
English
~ Cooperation and collaboration with internal and external stakeholders (customers and/or suppliers, subject to liability conditions)
~ Contribute as a unit representative in project teams
~ Ensure deliveries are made.
~ Part-time members, such as
~ Inform your partner or customer of the issue.
~ Ensure knowledge is acquired in relevant procedures. (Troubleshooting is available)
~ Technical orientation and training as a technical expert or cook. As a mentor for beginners and senior colleagues.
~ Identify and implement resource constraints and cost reduction functionalities
~ Demonstrate a positive work ethic and influence others
~ Ideas for designing and applying processes for continuous improvement when you are a professional/organisational team or a senior member.
~ Ensure compliance with Novartis and other relevant regulations
~ Consolidate results to enable data evaluation and draw conclusions
~ Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
~ Distribution of marketing samples (if applicable)
Key Performance Indicators
~This is a universal job description intended to capture some of the primary tasks of this role that are common to all functions or divisions. It is not intended to represent all specific responsibilities of the position ~ Organises, coordinates, monitors and executes activities related to the assigned area of responsibility. Ensures process compliance with multinational regulations, as well as Novartis internal procedures and GxP requirements.
Work Experience
~Professional experience (approximately 3-5 years) in a GMP and analytical environment (e.g. quality control)
Skills
~Material Requirements Planning (MRP)
~Material management
~Project management
~Supply chain planning
~Supply chain management
~Master data
~WMS (Warehouse Management Systems)
~Production planning
~Continuous improvement process
Language
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
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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