Jobs at BioMarin Pharmaceutical Inc.

Lead U.S. VOXZOGO brand strategy, competitive readiness, market execution, omnichannel campaigns, customer engagement, cross-functional alignment, agency partnerships, budget management, and KPI performance tracking. Drive growth and retention while collaborating with sales, medical affairs, market access, corporate communications, global marketing, senior leadership, and external stakeholders.

Partners with the U.S. Pompe and Fabry commercial organization to design, deliver, and scale compliant learning programs across onboarding, product and disease training, launch readiness, selling excellence, and ongoing capability development. The role translates brand strategy and scientific information into field-ready learning, manages MLR/PRB approval and audit readiness, uses performance metrics to optimize programs, and pilots AI-enabled and modern learning approaches. It also collaborates globally and cross-functionally with Marketing, Medical, Compliance, Market Access, HR, and field leadership.

Owns end-to-end global supply planning for biotech products from drug substance through finished goods. Integrates demand and supply, manages inventory strategies, monitors KPIs, mitigates supply risks, leads scenario planning, and coordinates with manufacturing, quality, regulatory, logistics, finance, commercial, and regional planning teams. Maintains planning data and parameters in SAP IBP while ensuring plan credibility, process compliance, product availability, and alignment with global supply strategies.

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 U.S. accounts payable operations, team development, outsourced processing, payment execution, reporting, month-end close, SOX compliance, and audit support. Drives global AP transformation through process standardization, automation, ERP enhancements, AI-enabled invoice processing, workflow optimization, and integration initiatives. Partners with Procurement, Treasury, Accounting, Supplier Management, Global AP, and Digital Technology teams to improve controls, scalability, service delivery, and operational continuity.

Leads commercial FP&A for BioMarin’s approximately $1B EUCAN region, serving as finance partner to the Regional SVP and leadership team. Oversees revenue planning, forecasting, performance management, OPEX, resource allocation, variance analysis, and executive decision support. Partners with commercial and finance stakeholders across countries, translates complex financial information into actionable insights, and leads, coaches, and develops a team of five finance professionals.

Supports biologics operations through technical writing, document management, and training administration. Develops and improves documentation strategies; drafts, reviews, and approves SOPs, protocols, reports, forms, work instructions, and BPDs. Ensures data integrity, ALCOA compliance, regulatory readiness, and effective use of Veeva Quality Documents and ComplianceWire. Collaborates with technical subject matter experts, manages document transitions and change requests, and supports training programs, guides, and e-learning materials.

Performs routine and non-routine analytical testing for drug substance and drug product process development, lifecycle programs, manufacturing, release, stability, and investigations. Executes chromatographic, electrophoretic, spectrophotometric, plate-based, and cell-based assays; analyzes data; documents work under GMP/GLP requirements; supports method qualification, validation, transfer, troubleshooting, laboratory readiness, regulatory inspections, and cross-functional technical activities.

Leads development, qualification, transfer, remediation, and lifecycle management of analytical methods for biologics, small molecules, peptides, and oligonucleotides. Focuses on glycan characterization, biophysical analysis, chromatography, capillary electrophoresis, and mass spectrometry. Supports product characterization, CMC development, comparability, control strategies, regulatory submissions, technical documentation, investigations, laboratory operations, and mentoring junior scientists.

Performs laboratory-based purification and analytical characterization of recombinant enzymes, proteins, antibodies, and peptides. Independently executes and optimizes chromatography and filtration workflows, troubleshoots equipment and processes, analyzes experimental data, maintains laboratory documentation, and communicates findings to multidisciplinary research teams. Supports analytical method development, technology transfer, instrument maintenance, and safe laboratory operations across early-stage biologics research programs.

Leads global digital strategy and capabilities for BioMarin’s International Business Unit. Develops omnichannel customer engagement strategies across web, paid media, SEO/SEM, email, CRM, social, and field tools. Owns digital roadmaps, customer journeys, segmentation, governance, agency relationships, budgets, measurement frameworks, dashboards, and marketing mix modeling. Partners with marketing, sales, analytics, IT, and digital operations to drive digital transformation, capability adoption, campaign performance, and customer-centric commercial outcomes.

Supports biopharmaceutical manufacturing operations, including cell culture, filtration, chromatography, centrifugation, protein purification, and formulation. Operates equipment, identifies processing issues, supports process optimization, writes and reviews procedures, and uses quality systems for deviations, CAPAs, and change requests. Participates in projects, metrics trending, and business system implementation while working rotating overnight shifts and performing physically demanding tasks in a cGMP environment.

Design and synthesize antibody-oligo, peptide, and other bioconjugates for nucleic acid therapeutics. Develop purification and conjugation methods, characterize products using HPLC, LC-MS, SDS-PAGE, and spectroscopy, and collaborate with Biology, Pharmacology, and Process Development teams on preclinical and clinical programs. Maintain laboratory documentation, present findings, and contribute scientific expertise to multidisciplinary research projects.

Performs internal audits assessing governance, risk, controls, compliance, fraud, waste, and operational effectiveness. Supports audit planning, scoping, testing, data analysis, documentation, reporting, stakeholder interviews, and issue escalation. Develops risk-control matrices, dashboards, reports, and continuous monitoring tools. Partners with cross-functional teams and management to identify root causes, validate findings, and improve business processes.

Manages monthly, quarterly, and annual financial reporting under US GAAP, IFRS, and local GAAP. Responsibilities include account reconciliation, profitability analysis, statutory reporting, audits, tax support, SOX controls, accrual analysis, outsourced provider management, and process improvement. The role partners with FP&A, finance teams, auditors, tax professionals, and global stakeholders while supporting ad hoc financial analysis and reporting.

Supports enterprise-wide contracting by researching prior agreements, drafting and negotiating contracts using approved templates and playbooks, tracking agreements through contract lifecycle management systems, and ensuring policy compliance. Serves as a liaison among Legal, procurement, business stakeholders, and external parties. Also supports legal department initiatives, user training, template maintenance, process improvements, and cross-functional projects.

Develops and operationalizes AI and machine learning solutions for biotech technical operations, including manufacturing, quality, engineering, and supply chain. Responsibilities include data acquisition, feature engineering, predictive modeling, GenAI and RAG solutions, MLOps, dashboards, data strategy, validation documentation, stakeholder collaboration, and mentoring. The role translates business problems into measurable AI use cases and ensures scalable, secure, regulated deployments.

Manage intellectual property docketing, file management, patent annuities, renewals, deadlines, and formal documents. Coordinate with attorneys, patent agents, outside counsel, and vendors to ensure accurate and timely filings, payments, and records. Support the IP team with administrative tasks and special projects while identifying opportunities to improve efficiency through technology and AI.

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.

Coordinates external contract manufacturing supply chain activities for clinical drug products. Manages ERP records, inventory, purchase orders, invoices, shipments, reconciliations, audits, reference standards, stability samples, and GMP master data. Partners with Supply Chain, Quality, MSAT, process owners, and CMOs to ensure material and finished-goods supply needs are met. Requires supply planning or inventory management experience, regulated manufacturing knowledge, and strong cross-functional communication.