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Internship for students as Global Clinical Artwork Manager - RiKO (m/w/x)
Creating and revising labeling artwork for investigational medicinal products, ensuring compliance with medical, legal, and regulatory requirements. University studies in pharmaceutical, biopharmaceutical, or Supply Chain Management required. 12-month internship with a global healthcare company.
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Anforderungen
- Enrolled or completed university/technical college studies (pharmaceutical, biopharmaceutical, Supply Chain Management) within last 12 months
- Interest in using knowledge in a 12-month internship
- Interest in getting to know the pharmaceutical industry
- Solid understanding of Pharma Supply Chain
- Solid understanding of clinical packaging processes
- High cultural awareness
- High social competence
- Cooperation and communication in complex cross-cultural situations
- Well-developed teamwork skills
- Well-developed collaboration skills
- Well-developed negotiation skills
- Problem-solving skills
- Decision-making skills
- High attention to detail
- Understanding of systems and technical designs
- Full application of Supply Chain theories
- Full application of Business Process theories
- Full application of cGMP theories
- Full application of Supply Chain principles
- Full application of Business Process principles
- Full application of cGMP principles
- Full application of Supply Chain techniques
- Full application of Business Process techniques
- Full application of cGMP techniques
- Adherence to procedures and standards in GMP environment
- Project management from initiation to delivery
- Ability to work independently
- Ability to set priorities
- Self-motivated
- Proactive
- Quick thinking
- Adaptable
- Clear and professional written communication
- Clear and professional verbal communication
- Excellent English skills
- Customer-focused
- Ability to create trustful relationships with business partners
- Ability to quickly learn a broad range of skills
- Confirmation from university for mandatory internship (Non-EU/EFTA citizens)
Aufgaben
- Create and revise labeling artwork for Investigational Medicinal Products
- Ensure label contents meet medical, legal, and regulatory requirements
- Manage the clinical label life cycle for various label types
- Represent the label team in cross-functional and production meetings
- Collaborate with internal and external partners to provide labeling solutions
- Participate in global and local projects to optimize Clinical Supply
- Lead projects to improve label processes and systems
- Communicate timelines and project updates to customers and partners
- Drive issue resolution in the label creation process
- Manage the label approval process with Label Representatives
- Evaluate and implement improvements to the labeling process using LPS principles
- Develop skills in software for label creation, such as SAP Global Label Management
- Maintain label master data in appropriate systems
- Order labels from vendors and monitor order status
- Monitor KPIs for team performance and vendor activities
- Develop ideas and initiate continuous improvements
- Manage supplier relationships and drive monthly performance reviews with vendors
- Participate in Service Level Agreement adaptations
- Act as main contact for booklet vendors regarding Roche label creation
- Support the New Capabilities Team in developing new label capabilities
- Coordinate development and testing of new label technologies with vendors
- Collaborate with the Artificial Intelligence Community of Practice
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Von Nejo automatisch aufbereitet
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