Supply Chain Manager - Global Clinical Supplies

Position Overview

Located in Basel, Switzerland, this role is integral to the Clinical Supply & Operations Planning (CS&OP) process. The successful candidate will be responsible for managing the entire supply chain process from Clinical Finished Goods (CFG) to Drug Substance (DS) and associated booklet labels, ensuring that demand fulfillment is met for designated projects.

Key Responsibilities

• Aligns supply strategies within Global Clinical Supplies (GCS) while contributing to supply strategies across CHAD/PHAD/Biologics.
• Engages in Global Project Management Meetings (GPMM) with Clinical Supply Planning Lead (CSPL) and Clinical Trial Supply Manager (CTSM) to ensure synchronized demand and supply.
• Ensures fulfillment of demand and oversees supply and regulatory compliance, representing GCS in TRD Sub-team discussions.
• Develops a manufacturing schedule that balances cost efficiency and flexibility, minimizing waste while addressing demand variations.
• Drives Long Term Demand and Capacity Planning (LTDP) in collaboration with various planning leads, adhering to Supply Chain Management KPIs.
• Manages operational performance metrics, focusing on excellence in supply planning.
• Utilizes data and digital tools within the supply chain domain, particularly in SAP for ordering and master data management.
• Implements Rapid Response (Maestro) for effective portfolio supply and demand planning.
• Collaborates with finance, customs, and compliance teams to establish a robust supply chain design for the portfolio.
• Drives change control strategies from a Global Clinical Supplies perspective.
• Assesses the impact on clinical supplies and contributes to regulatory submission planning.
• Integrates comparator supply strategies into procurement and release planning.

Qualifications

• A degree in science, engineering, or equivalent is required.
• Fluency in English is essential.
• A minimum of 5 years of practical experience in the chemical or pharmaceutical industry, or 3 years in a specialized area.
• Proficient knowledge of the drug development process and relevant regulations (e.g., GMP, HSE).
• Demonstrated project management expertise, with strong organizational and planning skills.
• Strong problem-solving abilities and creative thinking skills are vital.
• Excellent presentation, communication, negotiation, and interpersonal skills are crucial for team collaboration.
• Intermediate leadership skills are necessary.

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