Material Planner

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Our manufacturing and process development teams manage the production of our therapies for clinical trials and commercial markets. These engineers, technicians, scientists, and support professionals continually provide quality assurance and ensure we meet all regulatory standards. We have manufacturing facilities in Northern California and in Cork, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
Title: Material Planner
Work Type: Contract
Duration: 12 Months
Role
The primary role of the Material Planner is to ensure the availability of raw material components to meet the production schedule in Drug Substance, Drug Product and Finish Goods Packaging Operations. Ensure raw material components are planned, purchased and released within the guidelines established in the ERP SAP system. The Material Planner will play a key role in the development and implementation of systems and processes to ensure optimal raw material coverage in line with the Master Production Schedule as well as product launch activities.
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
Key Responsiblities:
Responsible for Material Requirements Planning (MRP) in line with the Master Production Schedule in SAP to ensure that operational requirements are met
Responsible for converting purchase requestions to purchase order as required by SAP detail schedule including payment of supplier invoices
Responsible for monitoring Materials release status to meet detailed schedule
Responsible for Inventory Management end to end including (Pricing (Purchase Info Record), Purchase Price Variance (PPV), reserve process, expiry, FIFO, FEFO, safety stock, lead times etc)
Responsible for issuing quarterly supplier forecasts
Responsible for generating and issuing recurring Heatmap/Material Readiness to site stakeholders. Participate in weekly material readiness activity.
Responsible for ensuring that supplier open order book is issued and aligned with SAP on a weekly basis.
Responsible for Master Data accuracy in SAP for material components
Responsible for aging receipts, resolving issues and identifying root causes
Responsible for Short Term Exception Management (STEM) program as required and proactively engage with stakeholders to resolve schedule conflicts.
Responsible for inputs into the monthly site Supply Chain Review meeting (SCR)
Participate in end of campaign performance review (Plan V Actual) to correct future campaign requirements
Participate in Global Category Form and Quarterly Business Review (QBR)
Participate in site Single Use Application strategy meetings
Member of the functional process team level as required
Facilitate Tier 1 Purchasing team meeting
Complete material planning scenarios as required to maintain detailed schedule
e as required in delivery of Change Request, CAPA ,Deviation & Supplier Change Notification (SCN) within the Quality Management System (QMS) system
Engage Right First Time (six-sigma) and lean manufacturing practices leading to Operational Excellence
Develop, maintain and publish KPI’s for supplier performance (OTIF)
Participate in Continuous Improvement (CI) projects
Safety and Quality
Standard Operating Procedures (SOP)
Participate in daily cross-functional meetings to ensure maintenance of Adherence to Schedule *(ATS) and Adherence to Plan *(ATP) in line with Make / Assess / Release commitments
Participate in weekly S&OE meetings ensuring cross functional alignment of plans
Participate in Material Planner Standard Work
Metrics
Cost Savings
Dual Sourcing
Operational Readiness Programs (ORP)
List above identify key responsibility, but other duties maybe require