Skip to main content


  • Manage the day-to-day Artwork activities within the FDF Business of Centrient Pharmaceuticals drug products (FDF’s) commercially produced and new products being developed. Optimization of the Artwork process of Drug Products with special focus to launch new products in time and an uninterrupted Artwork change for existing products.

Key Individual Accountabilities

  • Coordination and management of the artwork process between Customer and CMO during new product launch development as well as artwork changes required for running business.
  • Responsibility requires the artwork coordinator to be an intermediary between customer and CMO, where the customer develops the artwork and the CMO technically checks the artwork.
  • Responsible for clear communication between the different stakeholders and resolving any artwork related issues which arise.
  • Artwork needs to be managed within a timely manner, prioritizing in accordance with any due dates or implementation dates.
  • Monitor the Artwork processes per customer and CMO and inform key stakeholders on progress and bottlenecks.
  • Manage and maintain the artwork tracking tool.
  • Communicating implementation instructions to packaging site, including invalidation instructions for superseded artwork.
  • Maintaining and checking artwork costs related to destruction of excess or invalid packaging material at CMOs Responsible for progress reporting, KPI’s and informs MT monthly.
  • Escalating and providing support with any identified artwork issues.
  • Focus is working toward a standardization and optimization model of the artwork process between all sites and customers.

Key Shared Accountabilities

  • Attend S&OP meetings for running business.
  • Attend launch meetings for new customers and/or new CMO’s.
  • Instruct DSCM planner and BEMS on planning delivery in case of (new/changed) packaging materials for (new) customers, ensuring timelines are respected.
  • Comply to the company, SHE&Q and security regulations; signal unsafe situations, (near) incidents, environmental, quality and security risks, stop proceedings when serious violations of the regulations occur and report.


  • Minimum Graduate
  • At least 5 years of experience in Pharmaceutical industry.
  • Leadership & problem solving skills
  • Project management & Organizational skills
  • Knowledge and or experience in Artwork development / Artwork management in a pharmaceutical company
  • Ability to deliver to specific deadlines
  • Affinity with artwork programs such as Glams / Blue etc.


Truly global work environment.

High performance culture.

Ability to make a difference.

Best in class compensation.


Personal information

When submitting your message your personal data will be processed in accordance with Centrient's Privacy Statement. Please read the Privacy Statement here.


* this is a required field