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Associate Director - Product Artwork Management
BioMarin Pharmaceutical Inc.Associate Director managing product artwork for BioMarin's pharmaceutical portfolio. Leading strategy, compliance, and global readiness for artwork and labelling processes.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading product artwork management across the product lifecycle, with a strong focus on regulatory compliance and quality assurance in GxP environments. Proven ability to implement global strategies and manage cross-functional teams for successful product launches.
Highest-signal resume keywords
Artwork ManagementRegulatory FrameworksProduct Lifecycle ManagementCross-Functional LeadershipGxP Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Artwork Lifecycle ManagementProduct LaunchLabelling ProcessesPackaging OperationsQuality Assurance
Soft Skills
LeadershipStrategic PlanningCollaboration
Tools & Technologies
GLAMSVeeva Vault
Industry Keywords
PharmaceuticalBiotechGMPICHFDAEMA
Tech Stack
Tools & technologiesVault
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Equal Opportunity Employer/Veterans/Disabled
- Health insurance
- Retirement plans