The Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished
Good (CFG) to Drug Substance (DS) ensuring demand fulfillment for assigned projects. The SCM acts
as key contributor to the Clinical Supply & Operations Planning (CS&OP) process in TRD/BTDM/GCS
and provides transparency on supply constraints and manages related aspects accordingly within TRD
and BTDM.
Execute and monitor timely activities related to assigned area of responsibility under the guidance and
accountability of more senior associates.
YOUR KEY RESPONSIBILITIES:Your responsibilities include, but are not limited to:
1. Creates and maintains the end-to-end supply plan from CFG to DS. Harmonizes the supply strategy within GCS and contributes to the supply strategy of CHAD/PHAD/ BTDM.
2. Leads the Clinical Demand Planning Meeting (CDPM) ensuring alignment between demand and supply.
3. Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team/BTDM CMC meeting. Represent GCS at TRD Sub team/BTDM CMC on supply chain aspects.
4. Optimizes the inventory strategy at PP and CFG level together with CTSM. 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
5. Supports Long-term demand and capacity planning (LTDCP). Adheres to SCM KPI for project and unit. Manages ordering activities and master data requirements in SAP within the scope of the role
6. Drives the comparator sourcing activities and comparator blinding strategy. And also Oversees Comparator resupply strategy in support of budget planning
7. Provides impact assessment on clinical supplies and contribute to the regulatory submission strategy
8. Engages and contributes to the Clinical Packaging Execution Meeting (CPEM) to ensure alignment
with Operations and supply continuity
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum requirements
WHAT YOU’LL BRING TO THE ROLE:
Why consider Novartis?
799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at Novartis!
Commitment to Diversity & Inclusion:
Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.
Division
Global Drug Development
Business Unit
TECHNICAL R & D GDD
Country
India
Work Location
Hyderabad, AP
Company/Legal Entity
Nov Hltcr Shared Services Ind
Functional Area
Research & Development
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
No