Jobs at BioMarin Pharmaceutical Inc.

Maximize sales of BioMarin products across a multi-state territory by developing hospital and community healthcare accounts, executing business and institutional plans, identifying potential rare-disease patients, supporting therapy initiation and adherence, and building relationships with healthcare professionals and key stakeholders. The role requires territory financial management, disease education, internal collaboration, compliance, leadership, and 50–75% overnight travel with remote selling.

Leads governance, roadmap execution, lifecycle management, validation, release delivery, vendor oversight, and continuous improvement for BioMarin’s Veeva Vault RIM platform. Partners with Regulatory Affairs, R&D, Quality, technology teams, Veeva, and managed service providers to enable submissions, publishing, registrations, archival, integrations, reporting, automation, and AI capabilities. Ensures compliant system operations through change control, testing, documentation, risk management, and audit readiness.

Leads end-to-end value chain strategy and performance for pharmaceutical products across clinical and commercial stages. Owns supply, lifecycle, network, inventory, costing, risk mitigation, business continuity, and regulatory alignment. Leads matrixed cross-functional teams spanning planning, manufacturing, quality, procurement, logistics, finance, and commercial functions. Drives operating model design, continuous improvement, strategic investments, and executive governance while ensuring reliable, compliant, cost-effective patient supply.

Maximize sales of BioMarin products across a four-state PKU territory. Develop territory business plans, achieve sales and market-share goals, manage finances, educate healthcare professionals on PKU data, support patient compliance, coordinate care, and build relationships with geneticists, nurses, counselors, and other stakeholders. Lead through influence, participate in disease-awareness and professional-society activities, provide clinical-practice insights, and conduct both in-person and virtual customer engagement.

Leads global strategic sourcing and category management for BioMarin’s external contract manufacturing network. Responsibilities include CMO selection and due diligence, API sourcing, contract negotiations, supplier risk mitigation, supply chain resilience, executive reporting, and building a high-performing procurement team. The role partners with Quality, Manufacturing, Regulatory, Supply Chain, Technical Development, Finance, and External Operations teams while managing biologics and small-molecule manufacturing requirements.

Leads global Integrated Business Planning across demand, supply, inventory, capacity, financial objectives, and clinical-to-commercial transitions for a rare disease supply network. Owns IBP and S&OE processes, scenario planning, inventory strategy, long-range capacity modeling, analytics, governance, executive decision support, and cross-functional alignment. Manages and develops integrated planning professionals while driving planning maturity, technology adoption, risk mitigation, supply resilience, and patient-centric product access.

Leads field-based sales and account management for Galafold and Pombiliti Opfolda across Michigan and Indiana. Develops territory plans, drives demand and patient identification, engages specialty healthcare providers, supports treatment access, and delivers sales objectives. Partners with Clinical Coordinators, Market Access, Medical Affairs, and Marketing to address patient-care barriers, execute brand strategy, analyze territory performance, maintain forecasts, and ensure compliant customer engagement.

Serves as the lead finance business partner for Technical Development and Global Quality. Leads budgeting, forecasting, long-range planning, variance analysis, scenario modeling, investment evaluation, resource allocation, KPI development, and executive reporting. Partners with senior leaders and cross-functional teams to translate operational priorities into financial plans, assess risks and opportunities, oversee expenses and capital investments, and improve FP&A processes, systems, and reporting in a global biotechnology environment.

Advise stakeholders on Good Pharmacovigilance Practices compliance, assess regulatory and policy adherence, perform GVP and R&D audits, and support health authority inspection readiness. The role manages compliance risks, contributes to PSMF and REMS programs, improves the global GVP audit program, mentors junior staff, and partners across the organization on quality and compliance initiatives.

Manages a multi-state territory selling and educating healthcare providers about therapies for skeletal conditions. Responsibilities include achieving sales and patient-start targets, developing account business plans, building relationships with pediatric endocrinology, orthopedics, genetics, and referral providers, coordinating with clinical support and internal teams, supporting disease awareness, communicating clinical data, and maintaining compliance in a regulated biotech environment. Overnight travel of 40%–60% and occasional evening or weekend educational events are required.

Leads global product artwork and printed-labeling strategy across the pharmaceutical lifecycle. Builds standardized operating models, governance, GxP-compliant processes, inspection readiness, and digital systems. Oversees artwork changes, launches, regulatory compliance, quality events, CAPAs, vendors, KPIs, and cross-functional coordination across Regulatory, Quality, Manufacturing, Supply Chain, and Commercial teams. Manages and develops the artwork organization while driving process improvement, automation, data integrity, and right-first-time delivery.

Manage day-to-day external manufacturing operations at contract manufacturing organizations for clinical and commercial products. Responsibilities include production planning, supply issue resolution, CMO performance management, material movement, root cause analysis, dashboards, change controls, deviations, technology transfers, launches, validation, compliance, contracts, and operational readiness. Lead cross-functional teams and ensure compliant, uninterrupted product supply across biologics, small molecules, and finished-goods packaging operations.