Jobs at BioMarin Pharmaceutical Inc.

Manages BioMarin’s Montreal territory to achieve sales, market share, and profit targets for rare-disease therapies. Develops business plans, maintains relationships with healthcare customers, delivers product and disease education, represents the company at medical meetings, and coordinates promotional activities within regulatory guidelines. Collaborates with Medical Affairs, Market Access, and Marketing while traveling throughout Canada and occasionally internationally.

Provides quality assurance oversight for lot release and secondary packaging operations in a pharmaceutical manufacturing environment. Responsibilities include compiling lot release packs, conducting AQL inspections, reviewing deviations and CAPAs, supporting change controls, approving manufacturing inputs and SOPs, and driving process improvements. The role works cross-functionally with manufacturing, supply, maintenance, metrology, and quality control teams while ensuring GMP compliance, timely issue escalation, and a safe workplace.

Leads the QC Microbiology laboratory team at BioMarin’s Cork site, overseeing microbiological testing, environmental and utilities monitoring, sterility programs, investigations, reporting, compliance, equipment validation, inventory, and external laboratory relationships. The role manages staffing, training, performance, capacity planning, audits, inspections, budgets, and cross-functional coordination with Quality, Manufacturing, Facilities, Regulatory Affairs, and Supply Chain. It also supports contamination control strategies, continuous improvement, and global quality projects.

Supports BioMarin’s External Quality Systems program by monitoring quality metrics, coordinating deviation, CAPA, and change-control activities, managing governance meetings, delivering QMS training, supporting audits and inspections, and implementing continuous improvement initiatives. The role also partners with global quality teams, contributes to digital improvement projects, and helps standardize quality reporting and compliance processes across the organization.

Provides administrative, coordination, and operational support to Germany’s Commercial teams. Responsibilities include organizing events, coordinating contracts and approvals, managing budgets and purchase orders, arranging travel, maintaining compliance documentation, supporting office and fleet operations, and collaborating with Finance, Compliance, Legal, Marketing, and sales stakeholders. The role requires strong organization, communication, prioritization, multitasking, German and English fluency, and confident Microsoft Office skills.

Manages a Houston-based, multi-state territory promoting BioMarin’s rare-disease therapy to pediatric endocrinology, orthopedics, genetics, and referring physicians. Responsibilities include achieving sales and patient-start targets, clinical education, account planning, cold calling, stakeholder coordination, disease awareness, and compliant communication of clinical data. The role requires collaboration with clinical support, market access, compliance, and brand teams, plus 40%–60% overnight travel and occasional evening or weekend educational events.

Leads implementation and sustainment of 6S across biotechnology laboratories. Responsibilities include program coordination, workplace assessments, visual standards, audits, action tracking, training, coaching, performance reporting, data analysis, and change management. Partners with laboratory teams, scientists, engineers, EHS, Facilities, and leadership to improve safety, compliance, workplace organization, operational flow, and continuous improvement.

Supports medical facilities and healthcare stakeholders across Turkey by providing scientific education, clinical and technical support, patient identification, treatment guidance, and product administration training. Builds relationships with physicians, pharmacists, investigators, and opinion leaders; supports investigator-sponsored studies, adverse-event processes, cold-chain requirements, advocacy initiatives, and scientific forums. Monitors clinical and competitive developments while delivering product presentations and collaborating with medical, research, access, and commercial teams.

Owns and supports U.S. controllership accounting activities, including journal entries, reconciliations, audits, SOX controls, SEC filing schedules, and cross-functional initiatives. Provides guidance to junior accountants, evaluates transactions under U.S. GAAP, and improves accounting processes through automation, reporting enhancements, and technology solutions. This hybrid role requires onsite work in San Rafael twice weekly.

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.

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.

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.

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.

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.

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.

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.

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.

Develops Japanese regulatory strategies and leads JNDA, JsNDA, post-marketing, re-examination, JAN, and expedited pathway submissions for pharmaceutical products. Serves as the primary liaison with MHLW and PMDA, leads agency meetings, evaluates regulatory changes, and supports clinical development strategy in Japan. Collaborates with global and regional teams to align strategic and operational deliverables.