
Key ResponsibilitiesThe Associate Director, End‑ to‑ End Planning capabilities is responsible for defining, governing, and evolving BioMarin’s end‑ to‑ end supply chain planning framework across demand, supply, inventory, production, and network planning. The role ensures the planning framework enables alignment between commercial demand, manufacturing capacity (Drug Substance, Drug Product, Finished Goods), inventory strategy, and financial commitments, supporting consistent, high‑ quality decision‑ making across the enterprise.Operating as an enterprise‑ level individual contributor, this role establishes clear decision rights, standardized planning routines, and disciplined governance mechanisms across functions, regions, and manufacturing sites. Partnering closely with Commercial, Manufacturing, Quality, Regulatory, Finance, IT, and external partners, the Associate Director strengthens the effectiveness of BioMarin’s multi‑ site global manufacturing network and supports ERP and advanced planning system transformation, enabling continued maturation toward an integrated S&OP / IBP operating model.End‑ to‑ End Supply Chain Planning Process capabilities
Demand Planning
Supply & Production Planning (Drug Substance, Drug Product, Finished Goods)
Inventory Planning and Optimization
Network Design, Capacity, and Constraint Management
Define and institutionalize global process standards, including end
‑ to‑ end process flows, operating models, governance forums, and documentation (SIPOC, RACI, SOPs, playbooks).S&OP Process Design and Governance
Performance Management, Insights, and Continuous Improvement
Systems Enablement and Data Governance
Cross‑ Functional and Network Collaboration
Transformation and Change Leadership
Required Qualifications
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.
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery. The company develops and commercializes targeted therapies that address the root cause of the genetic conditions that it seeks to treat, helping to better the lives of those struggling with rare genetic disease. BioMarin discoveries have led to eight first or best-in-class commercial treatments and a pipeline of multiple product candidates applying the same science-driven, patient-forward approach to broader group of genetic disorders. The more innovative solutions developed, the more lives BioMarin can impact.
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