Job type full-time
Full job description
2025! this is the year that global clinical supply is targeting for completing the evolution our systems into a “digital enabled” landscape of 300+ associatesJoin a team of globally collaborative colleagues at the ‘global clinical supply (gcs)’ function to support clinical trials from phase 1 to approval and be a key interface between technical research & development (trd) teams and the clinical teams!
At gcs, we aspire to become a data and digital powered, resourceful, agile organization to deliver more products to more patients efficiently, through empowered and highly capable teams.
Your key responsibilities will include but are not limited to:
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/biologics
Leads the clinical demand planning meeting (cdpm) 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 meetingRepresent gcs at trd sub-team on supply chain aspectsOptimizes 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
Drives long term demand and capacity planning (ltdcp) coordinating with the cspl, dppl, dspl and tpl.
Adheres to scm kpi for project and unit, data and digital savviness in sc domainManages ordering and master data requirements in sap within the scope of the role
Drive the change control strategy for clinical supplies from gcs perspectiveProvides impact assessment on clinical supplies and contribute to the regulatory submission strategy.
Integrates comparator supply strategy into the trd procurement, blinding & release planning
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.
>5 years of practical experience in chemical / pharmaceutical industry
Good expertise in related field.
Good knowledge about the drug development process
Basic project management, good organization and planning skills
Knowledge of relevant regulations (e.g., gmp, hse etc.) and novartis specific standards.
Demonstrates problem-solving and idea generation skills
Good presentation skills, fundamental leadership skills.
769 million lives were touched by novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovationThat a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibilityAnd we can reinvent what`s possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challengesBecause the greatest risk in life, is the risk of never trying! imagine what you could do here at novartis!
Commitment to diversity & inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join our novartis network : if this role is not suitable to your experience or career goals but you wish to stay connected to hear more about novartis and our career opportunities, join the novartis network here: https://talentnetwork.novartis.com/network
Global drug development
Technical r & d gdd
Nov hltcr shared services ind
Research & development
Posted 4 days ago