Chiesi Group OverviewBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years of experience, operating in 30 countries with more than 6,000 employees. The Group is committed to improving people's quality of life by developing innovative drugs in key therapeutic areas.We are proud to be the largest global pharmaceutical group awarded B Corp Certification, recognizing our high social and environmental standards. We promote transparency, ethics, diversity, inclusion, and equal opportunities across our global family.Manufacturing DivisionChiesi Group has three production plants:Parma, Italy: The strategic hub for production and distribution, including a new Biotech Centre of Excellence launching in 2024 for monoclonal antibodies, enzymes, and proteins.France: Specializes in Dry Powder Inhalers and Metered Dose Inhalers, managing local distribution and exports.Brazil: Produces pressurized solutions, suspensions for inhalation therapy, and nasal sprays for the European market. A new facility in Italy is planned for 2025, focusing on inhalers and biological products.Position: Artwork Support SpecialistWe are seeking a collaborator to support artwork management within the Global Quality Operations team, based in Parma, Italy. The role involves operational support for artwork processes, collaborating with internal teams and external providers.Main ResponsibilitiesManage graphic activities for products across all countries with Chiesi affiliates or partners.Coordinate and involve stakeholders internally and externally for printed materials.Analyze data and files needed for artwork preparation.Verify artwork compliance with production and regulatory standards.Manage, upload, and monitor draft and approved files in the system.Ensure secondary packaging materials comply with approvals and supply chain requirements.Gather information on new product launches and coordinate launch activities.Support product launches and lifecycle management in collaboration with supply chain teams.Participate in regulatory inspections as needed.Monitor KPIs and update procedures accordingly.Experience & EducationMinimum 3 years in the pharmaceutical industry, with at least 1+ years in Quality departments.Master’s degree in a scientific field (e.g., Engineering, CTF, etc.).
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