Hybrid Artwork Specialist (Lisbon, Portugal) bei Grünenthal

Job Grade: PT10F 

Hiring Manager: Alexandra Lopes 

Internal Posting Date:  - 

​Professional  |  Permanent  |  Full-time  |  Hybrid​

Our people in Manufacturing & Global Operations share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain – from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future.

What the job looks like

Each day you’ll enjoy a variety of challenges, such as:

• Management of artworks for regulatory and technical changes affecting printed packaging materials e.g., labels, leaflets, folding boxes, foils etc.) for Grünenthal and Clients products’ portfolio;
• Diligent check of the correctness/compliance of the created artworks in multilingual files;
• Proper archive and diligent share of final approved master artworks with the respective business functions;
• Maintenance of packaging material master data and bill of materials in the relevant systems;
• Cross functional collaboration to ensure the timely delivery of quality artwork in an international environment (across regions);
• Monitor implementation of label changes for GRT products, according to regulatory timelines;
• Support new business integrations with strategy and planning concerning artworks;
• Creation, maintenance and archiving of standard operating procedures (SOP), packaging documentation and GMP-relevant documents.

What you'll bring to the table

To make the most of this role and truly thrive, you should have:

• High school degree or graduation in life sciences;
• Minimum 2 years experience in pharmaceutical industry areas such as Regulatory Affairs, Supply, Quality, Production;
• Previous experience in artwork development for pharmaceutical industry (preferred) or equivalent industry (e.g., Medical Devices, Cosmetics);
• Good verbal and written English. German and Spanish language skills are an advantage;
• Good knowledge of MS Office and SAP (preferred);
• Good knowledge of regulatory terminology and labeling guidelines;
• Basic knowledge of GMP regulations and guidelines.

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