Associate Director, Product Artwork Management
Listed on 2026-09-22
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Management
Operations Management, Regulatory Compliance Specialist, Business Analyst, Project & Program Management -
Business
Operations Management, Regulatory Compliance Specialist, Business Analyst
Who We Are
Bio Marin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options.
More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world‑class manufacturing capabilities. At the heart of Bio Marin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical OperationsBio Marin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain Bio Marin’s cutting‑edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
Role OverviewThe Associate Director, Product Artwork Management leads the end‑to‑end product artwork capability across the product lifecycle — from development through commercialisation and lifecycle management. The role moves the function beyond day‑to‑day execution to set strategy, design and scale fit‑for‑purpose processes, and establish the governance that ensures accurate, compliant, and on‑time delivery of printed packaging components (labels, cartons, leaflets) for every market Bio Marin serves.
Leveraging deep regulatory and quality expertise, the Associate Director defines the operating model, embeds inspection‑ready governance, and develops the team to deliver world‑class artwork performance. The role is the single functional lead for product artwork across the combined Bio Marin product portfolios, and the artwork and labelling subject‑matter expert and cross‑functional integrator across Regulatory Affairs, Quality, Technical Operations, Supply Chain, Manufacturing, and Commercial — enabling successful launches and uninterrupted supply to patients.
This is a build‑and‑grow mandate: the Associate Director is accountable for maturing artwork management from individual product ownership into a standardised, scalable, and governed function, and for developing a high‑performing team recognised as world‑class in artwork management.
Key Accountabilities Artwork Strategy & Operating Model- Define, scale, and implement a global printed‑labelling (artwork) strategy and implementation process spanning the combined Bio Marin product portfolio across all markets, aligned to company growth and the launch pipeline.
- Build out standardised, fit‑for‑purpose processes, standards, and ways of working across products, regions, and partners.
- Establish clear decision rights, prioritisation frameworks, and escalation pathways for artwork demand and change.
- Shape the multi‑year roadmap for artwork capability, systems, and digital enablement — including enterprise‑wide and AI‑driven transformation initiatives.
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