Accomplished Tactical Planner and S&OP Facilitator at Sandoz, A Novartis Division, adept in SAP ERP and MES WERUM, with a proven track record in enhancing supply chain efficiency through strategic capacity planning and lead time reduction. Excelled in master data management, contributing to a successful MRP II Class A project implementation. Demonstrates strong leadership in driving process optimization and fostering team collaboration.
• Review forecast for 24 months
• Prepare mid-term (24 months) production plan for S&Op Supply Review inputas Supply Plan
• Facilitate conflicts between processes and proposing medium/long termoptions in terms of optimization of capacity utilization;
• Ensure coherence with agreed budget/RF and site objectives, in terms ofutilization/shift configuration and resources;
• Propose the best supply plan to the Site Leadership Team during MonthlyBusiness Review.
• Review demonstrated capacity and rough cut capacity plan• Ensure demand fulfilment and adherence to committed dates• Maintain planning parameters in SAP Master Data
• Suport transfers and life cycle events;
Part of implementation team of Full Electronic Batch Record functionality in the Manufacturing Execution System (WERUM PAS-X), (Packaging Part);
• Creation and maintenance of Master Batch Record (MBR) in the MES system;
• BOM maintenance in ERP SAP
• Determining and maintaining in the system the correct values for routings,based on Demonstrated Capacity.
• Part of implementation team of Deviations and Quality Events ManagementSystem Trackwise;
• Part of implementation team of Product Serialization
Part of implementation team of MRP II Class A project implementation asWork Stream leader in Master Data Management
• Successful project implementation and MRP II Class A certified
• Leading master data team to implement MRP II requirements as statedin NOSSCE manual and achieve/sustain Class A in Novartis operationalstandards for supply chain excellence
• Overall process design for management of Master Data within SAP: formaldata creation and change control process;
• Building the Local Master Data Dictionary as reference document;
• Developing KPI calculation
Supervising of production activities of antibiotic products in the followingpharmaceutical forms: tablets, capsules and oral suspensions;
▪ Supervision of primary and secondary packaging operations ;
▪ GMP training of production personnel;
▪ Ensure compliance with GMP norms in shop floor;
▪ Ensure compliance with GDP norms in documenting;
▪ Investigating deviations, RCI and CAPA determination;
▪ Creation and revision of standard operating procedures;
▪ Staff organization;
▪ Orders/returns of raw materials and primary and secondary packaging from/to the warehouse;
Pharmaceutical Industry
OPEX
Lean Six Sigma
SAP ERP
MES WERUM
Production Master Data; BOM, Routing, Work Centers
Master Batch Record
Capacity Planning
Lead Time Reduction
MOQ strategy
Kinaxis / Rapid Response
MRP II
RCI, CAPA
Deviation Management
Demonstrated Capacity
KPI reporting