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.
Role Scope:
The Value Chain Product Leader is accountable for designing,, and continuously improving a bestinclass, endtoend value chain that reliably connects patients to medicines. This role provides focused,accountability for the product value chain within a defined scope, ensuring alignment to product strategy, enterprise standards, and regulatory requirements.As a matrix leader, the Value Chain Product Leader leads thefunctionalrepresentsfordevelopmentcost-effectiveThe Value Chain Product Leader proactively manages risk, drives lifecycle and network strategies, and leads mitigation when patientlevel supply risks are, including supply assessments that inform Global Issue Management and regulatory notification decisions.Key AccountabilitiesEnd-to-endOwn the design, performance, and continuous improvement of the product value chain, aligned to enterprise strategy and standards.Ensure reliable supply of qualityto patients across clinical and commercial stages.Deliver products to marketsdefined service andtargets.Product Lifecycle & Strategy ExecutionDrive the product lifecycle management roadmap,lead time, cost, and resilience.Define and execute product and network strategies, including flow of goods, SKU strategy, and inventory strategy.Identifyrequiredlong-termRisk Management & Business ContinuityProactively, assess, and communicate risksproduct quality, compliance, patient supply, and business continuity.Lead mitigation strategies and escalation for actionable supply risks, includingstockout scenarios.Own business continuity, supply chain efficiency, and agilityto ensure programare met.Financial & Performance ManagementOwn inventory health, key supply chain cost drivers, and‑offsEnsureproduct costing, including development and maintenance of standard costs.Enable,decision making across the value chain.Governance & Business PartnershipServe as the primary voice of the product in relevant business forums, including brand reviews, regional reviews, and portfolio governance.Define the target operating model for the product value chain, including roles, processes, and decision rights across Planning, Manufacturing, Quality, Logistics, and external partners.Build strong strategic partnerships with Commercial, Clinical, Technical Operations, and Enterprise functions.Leadership ResponsibilityThe Value Chain Product Leader is a matrix leader responsible for leadingteams accountable for executing product value chain strategies within their respective functions.The role provides coaching and development to team members on product and value chain requirements, monitors performance against deliverables, and provides feedback to functional management on individual performance and development needs.Key InterfacesTOPS Product TeamsSupply Planning & Demand PlanningClinical Supply Chain OperationsCommercial & Clinical OperationsManufacturing & Material OperationsProcurement & Category ManagementEnterprise Master Data ManagementLegal, Tax, Product Costing & FinanceLogisticsProduct Development & FormulationPackaging Development & ValidationEnvironmental Health & SafetyGlobal Trade ComplianceQuality Control & Quality AssuranceQualified Person / Responsible PersonProduct Artwork & Launch ManagementMinimumBachelor’s degree (BS/BSc) in life sciences, engineering, supply chain, or business administration, with 8–12+ years in materials management/production planning/scheduling, 5–10+ years in GMP/GCP compliant pharmaceutical operations, and 2–5+ years leading global, cross functional, matrixed teams.Strong supply chain and value chain management,expertiserisk.Demonstrated capability to assess issues across Regulatory, Quality, Supply Chain, and Manufacturing perspectivesE‑levelinfluenceleadership,‑culturalimprovementWrequiredNice to HaveMBA (Supply Chain, Finance, or Business Operations preferred)APICS or equivalent supply chain certificationLean / DMAIC certification (Green Belt or higher)PMP or equivalent project management certificationBiopharmaceutical operations experienceStrong financial and business acumenAdvanced regulatory and GMP, including ICH Q8–Q12
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.
