Associate Director - Product Artwork Management

🕒 July 14

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BioMarin Pharmaceutical Inc.

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1997

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 Post-IPO Debt on 2020-05

Healthcare • Biotechnology • Pharmaceuticals

BioMarin Pharmaceutical Inc. is a leading global biotechnology company dedicated to transforming genetic discoveries into innovative medicines. Founded in 1997, the company has developed eight marketed products that address life-threatening genetic and lysosomal storage disorders such as achondroplasia and severe hemophilia A. BioMarin is also heavily invested in research and development, with a robust pipeline of investigational medicines at various clinical trial stages. The company's mission revolves around improving patient care by leveraging scientific expertise to understand the underlying causes of these conditions. BioMarin is committed to inclusivity and patient advocacy, engaging closely with communities to enhance care and quality of life for those with rare conditions.

📋 Description

• The Associate Director, Product Artwork Management leads the end-to-end product artwork capability across the product lifecycle • Define, scale, and implement a global printed-labelling (artwork) strategy and implementation process spanning the combined BioMarin product portfolio across all markets • Shape the multi-year roadmap for artwork capability, systems, and digital enablement • Establish, own and maintain the artwork governance framework, ensuring accurate, compliant, and inspection-ready artwork across the portfolio and all markets • Lead artwork planning and readiness for new product introductions and global launches, with integrated timelines aligned to regulatory and supply milestones • Manage the artwork lifecycle from concept to implementation—ensuring right-first-time quality and compliant, traceable operations

🎯 Requirements

• Bachelor’s degree in Life Sciences, Engineering, Supply Chain, or related field; advanced degree (MBA, MSc) preferred • ~10–12+ years in pharmaceutical/biotech operations, with focus on artwork/labelling, product launch, or supply chain in GxP-regulated environments • Proven experience leading global, cross-functional programmes and building or transforming an operating model • Strong command of regulatory frameworks (GMP, ICH, FDA, EMA), product lifecycle and labelling processes, packaging operations, and labelling/artwork systems (e.g. GLAMS, Veeva Vault)

🏖️ Benefits

• Equal Opportunity Employer/Veterans/Disabled • Health insurance • Retirement plans