.Who we areAt Teva we are all in for better health for our patients, our society, and our planet and for our people. TEVA is one of the pharmaceutical companies that treats the most patients in the world, 200 million every day, and its differential element is its participation in the entire medication cycle. We achieve all this by producing and developing affordable medicines through high-quality processes, as well as specialized and innovative medicines, and active pharmaceutical ingredients. An important part of its global production is carried out in Europe, placing the patient at the center of everything TEVA does and with a firm, transparent and ethical commitment to society and the environment.Medis, established in 1985 and headquartered in Iceland with a global workforce of 130+ employees, specializes in out-licensing generic pharmaceutical dossiers developed by Teva R&D to third parties. Our services include supporting customers in obtaining marketing authorizations under their own name and supplying them with high-quality generic pharmaceutical products manufactured by Teva. As an industry leader in out-licensing, we provide a reliable source of intellectual property through our comprehensive registration dossiers that adhere to market regulations. With a portfolio of over 185 high-quality generic products in various forms, we offer full regulatory support, demonstrating a proven track record in securing approvals before patent expiries, allowing customers to acquire marketing authorizations in 140+ countries. Leveraging Teva's robust development, extensive manufacturing capabilities, and in-house expertise, we operate as a fully integrated entity to facilitate these services.The opportunityThis role offers an opportunity to lead serialization activities and initiatives within Medis. Your main objective will be to ensure compliance with serialization regulations, maintain uninterrupted supply, and enhance supply service levels.Please note this role is NOT a People Manager role. You will be an individual contributor to the teamLocation: Teva Madrid offices. We have a hybrid approach to home working!How you'll spend your dayLead serialization activities and initiatives.Ensure exceptional service levels and provide in-depth technical support in serialization aspects to assist clients throughout the serialization process and address specific market requirements.Onboarding and validation of new partners in Tracelink.Manage Serialization Master Data (MD), including gathering, verifying, and maintaining MD at product and partner levels.Proactively monitor product launches and open orders to ensure correct serialization coding and preparation.Coordinate with various departments to minimize serialization impact to supply timeframe.Maintain and enhance business processes and SOPs to streamline the serialization.Ensure business continuity and growth in new markets as the serialization regulations expert for multiple territories
