Supply Chain Manager - Global Clinical Supply
Sandoz GmbH
Supply Chain Manager - Global Clinical Supply
Summary
Location: Schaftenau, Austria, onsite.
Role Purpose: The Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) and Booklet labels, ensuring demand fulfillment for assigned projects. The SCM acts as key contributor to the Clinical Supply and Operations Planning (CS&OP) process in TRD/GCS and provides transparency on supply constraints and manages related aspects accordingly within TRD.
Has operational end to end responsibility for assigned activity. Leads and manages all project and local network activities and participates in cross-functional teams.
About the Role
Major accountabilities
- Harmonizes the supply strategy within GCS and contributes to the supply strategy of CHAD, PHAD and Biologics.
- Participates in the GPMM along with the CSPL and CTSM ensuring alignment between demand and supply.
- Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team CMC meeting. Represents GCS at TRD Sub-team on supply chain aspects.
- Actively contributes to the portfolio manufacturing schedule alignment from DS to CFG. Defines most cost-efficient ordering levels from CFG to DS, minimizing waste and allowing flexibility to accommodate demand variability.
- Drives long term demand and capacity planning coordinating with the CSPL, DPPL, DSPL and TPL. Adheres to SCM KPIs including the one being part of the SPE for project and unit.
- Proactively manages and adheres to functional performance indicators with a focus on supply planning excellence.
- Data and Digital savviness in supply chain domain. Manages ordering and master data requirements in SAP within the scope of the role.
- Adapt and implement Rapid Response (Maestro) for portfolio supply and demand planning, network design and scenario building.
- Establish the supply chain design in alliance with Funds Flow, Customs and Trade Compliance and TRD sub-team for portfolio.
- Drive the change control strategy for clinical supplies from GCS perspective.
- Provides impact assessment on clinical supplies and contribute to the regulatory submission strategy.
- Integrates Comparator supply strategy into the TRD procurement, blinding and release planning.
Minimum Requirements
- Degree in science, engineering or equivalent.
- Fluent English.
- More than 5 years of practical experience in chemical or pharmaceutical industry or more than 3 years of experience in field of expertise.
- Good expertise in related field.
- Good knowledge about the Drug Development process.
- Basic project management, good organization and planning skills.
- Knowledge of relevant regulations, for example GMP and HSE, and Novartis specific standards.
- Demonstrates problem-solving and idea generation skills.
- Good presentation skills.
- Intermediate Leadership skills.
- Very good communication, negotiation and interpersonal skills. Ability to work in interdisciplinary teams.
In accordance with Austrian law, Novartis is obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is 65.504,54 Euro per year on a full time basis. The actual salary will be significantly higher, as Novartis strives to maintain a competitive position in the market and considers previous experience, qualifications and individual competencies.
Why Novartis
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people collaborating, supporting and inspiring each other. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards
Learn about all the ways Novartis helps employees thrive personally and professionally. Read our handbook
Vollzeit
Forschung & EntwicklungLogistik & EinkaufLogistik & Supply Chain Management
€4.678
Sandoz GmbH
um mit der Karte zu interagieren.
Supply Chain Manager - Global Clinical Supply
Sandoz GmbH
Supply Chain Manager - Global Clinical Supply
Summary
Location: Schaftenau, Austria, onsite.
Role Purpose: The Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) and Booklet labels, ensuring demand fulfillment for assigned projects. The SCM acts as key contributor to the Clinical Supply and Operations Planning (CS&OP) process in TRD/GCS and provides transparency on supply constraints and manages related aspects accordingly within TRD.
Has operational end to end responsibility for assigned activity. Leads and manages all project and local network activities and participates in cross-functional teams.
About the Role
Major accountabilities
- Harmonizes the supply strategy within GCS and contributes to the supply strategy of CHAD, PHAD and Biologics.
- Participates in the GPMM along with the CSPL and CTSM ensuring alignment between demand and supply.
- Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team CMC meeting. Represents GCS at TRD Sub-team on supply chain aspects.
- Actively contributes to the portfolio manufacturing schedule alignment from DS to CFG. Defines most cost-efficient ordering levels from CFG to DS, minimizing waste and allowing flexibility to accommodate demand variability.
- Drives long term demand and capacity planning coordinating with the CSPL, DPPL, DSPL and TPL. Adheres to SCM KPIs including the one being part of the SPE for project and unit.
- Proactively manages and adheres to functional performance indicators with a focus on supply planning excellence.
- Data and Digital savviness in supply chain domain. Manages ordering and master data requirements in SAP within the scope of the role.
- Adapt and implement Rapid Response (Maestro) for portfolio supply and demand planning, network design and scenario building.
- Establish the supply chain design in alliance with Funds Flow, Customs and Trade Compliance and TRD sub-team for portfolio.
- Drive the change control strategy for clinical supplies from GCS perspective.
- Provides impact assessment on clinical supplies and contribute to the regulatory submission strategy.
- Integrates Comparator supply strategy into the TRD procurement, blinding and release planning.
Minimum Requirements
- Degree in science, engineering or equivalent.
- Fluent English.
- More than 5 years of practical experience in chemical or pharmaceutical industry or more than 3 years of experience in field of expertise.
- Good expertise in related field.
- Good knowledge about the Drug Development process.
- Basic project management, good organization and planning skills.
- Knowledge of relevant regulations, for example GMP and HSE, and Novartis specific standards.
- Demonstrates problem-solving and idea generation skills.
- Good presentation skills.
- Intermediate Leadership skills.
- Very good communication, negotiation and interpersonal skills. Ability to work in interdisciplinary teams.
In accordance with Austrian law, Novartis is obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is 65.504,54 Euro per year on a full time basis. The actual salary will be significantly higher, as Novartis strives to maintain a competitive position in the market and considers previous experience, qualifications and individual competencies.
Why Novartis
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people collaborating, supporting and inspiring each other. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards
Learn about all the ways Novartis helps employees thrive personally and professionally. Read our handbook
VollzeitForschung & EntwicklungLogistik & EinkaufLogistik & Supply Chain Management €4.678Sandoz GmbH
um mit der Karte zu interagieren.
