Erik Hansen Email & Phone Number

Novato, California, United States

-Develop production requirements based on patient demand. Partner with colleagues across all DS/DP/FG operations ensuring capacity and materials are available to support production operations.-Govern and lead the batch flow program at both strategic and tactical operations levels, striving to achieve the most effective and efficient process across the site.-Support the Global Sales and Operations Planning (S&OP) program in creating an integrated operational plan that supports the BioMarin business and Patent objectives.-Develop process metrics for Make/Assess/Release that measure effectiveness towards achieving goals, provide visibility to improvement opportunities, and track progress of improvement initiatives.-Support and partner closely with the MFG, Quality, Novato Technical Support, Engineering, Regulatory, Supply Planning, GEO, Network Strategy, and Capital Project groups.-Represent Novato Supply Chain in critical meetings (local and global)-Strong focus on visual management boards for all Novato Make/Assess/Release measures and status with particular focus on Novato Batch Board and Distribution Bulk Shipment Board.-Develop and/or support local and global programs/initiatives to deliver transformational change and/or continuous improvement across our processes and KPI’s.-Proactively engage stakeholders to solicit production plan scenario requests and resolve schedule conflicts.-Develop SME capability in Oracle EBS, BioG, and ASCP suite.-Proactively troubleshoot complex issues in Oracle data management by collaborating with Supply Chain SME’s locally and globally.-Lead and collaborate with site detailed schedulers and Operational Readiness Planner to align a strategic production plan with detailed campaign scheduling.-Build effective cross functional relationships with key stakeholders both internally and externally, including CMO operations. -Align with strategies and realization of company, site, and functional goals

Oversight and responsibilities of the end-to-end process for Raw Materials, which is included but not limited to the following:- GMP Gowning management- Master Cell Bank management- Forecasting of indirect raw materials for the Novato Site- Vendor managed inventory- Direct GMP raw material release (SCN, on-time testing, sampling, etc)- Miscellaneous support items- Third Party warehouses- Bulk Dispersion Management· Develops and executes replenishment strategies; conducts physical inventories and leads cycle counts.- Reviews for trends- Actively investigates result discrepancies- Reports results to stakeholders· Delegates and verifies the removal of expired raw materials and expired in-process inventory.· Manages and reports key metrics to drive Inventory cost savings such as scrap reduction, excess and obsolete, expiry, inventory levels, etc…· Complies with, authors, and enforces SOX (Sarbanes-Oxley Act) requirements, cGMP Documentation, Practices and Regulations.· Ensures accountability of inventory through transaction documentation, process and procedure verification, and system review.· Leads operational excellence initiatives to optimize business process and procedures/drive cost savings.· Manages raw material shortage/stock out by minimizing impact and coordinates action plan to ensure continuous supply.· Coordinates and provides Support for Supplier Change Notifications· Provides data analysis for production planning

Novato, California

• Receive and warehouse GMP raw materials, components and supplies per established SOP’s• Transport and distribute approved GMP raw materials, components and supplies to the designated manufacturing facilities• Transport all GMP in-process solutions to and from the designated manufacturing facilities• Maintain accurate inventory records for approved GMP raw materials, components and supplies• Perform cycle counts of approved GMP material inventory as assigned• Compliance with EH&S safety guidelines, especially those directly related to the operation of warehousing equipment such as pallet jacks and forklifts• Assist with the shipping of Approved Final Bulk Drug Substance to contract filling sites• Assist with the shipping of Clinical materials to outside sites as required• Assist with other tasks as required• Utilized excel knowledge to help in the transition to an In-suite Min/Max operation successfully. • Maintained safety processes and implemented new safety process improvements to reduce risk. • Developed changeover presentation for department assisting to proceduralize the different campaigns to minimize contamination risk, and inventory inaccuracies.• Produce and maintain KPI metrics for tracking of all raw materials with an emphasis on costs, and waste.

Vacaville, California

• Technician in the Centralized Manufacturing Services/Production Services (CMS/PS) Department• Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in current Good Manufacturing Practices environment. • Maintain areas in high state of inspection readiness via 5S/FIT.• Utilize business systems for inventory and process management, including proficiency in SAP - ordering/returning material and transferring of materials/kits/assemblies.• Participate in the support of production of mammalian cell cultures products within the Vacaville Facility. • Provide support to Manufacturing and Quality Control. • Duties include: Clean in Place/Steam in Place of freeze/thaw and portable tanks.Clean, assemble, and autoclave fermenters.Autoclave solutions and assemblies.Perform weighing and dispensing of materials.Handle and aliquot hazardous materials.Clean all associated parts needed for Upstream and Downstream operations. Assemble and autoclave filter assemblies for Upstream and Downstream operations.Provide quality materials and service to our customers.• Highly proficient in Human Machine Interface (HMI), Distributed Control System (DCS), Online review tool (OLRT) and Production Operations Management Systems (POMS).• Knowledge of Trackwise and applicable systems. • Participated in multiple Kaizen's to significantly reduce the number of human errors incurred in key processes. • Created and delivered multiple department wide presentations for training corrective behavior purposes.

Education record

Education record

Activities and Societies: Varsity Tennis. Mass Media.