Swiss Regulatory Affairs Specialist

Job description

Your Role Working in a Pharma team, you will be supporting the EMEA divisions on topics around the supply of raw materials into the pharmaceutical industry including regulatory, legal, compliance, quality and product safety responsibilities Responsibilities: Your responsibilities will bei: Completion of technical and regulatory documentation and information requests from customers for supply of raw materials into the pharmaceutical industry (questionnaires, supply chain agreements, quality agreement and technical agreements) in and English. Sourcing information internally and from suppliers to satisfy customer requests. Reporting and documenting customer requests via KPIs. Collaborating with commercial and value-added services teams, proactively leading and managing regulatory topics related to customer projects. Collaborating with QHSE & supply chain teams to ensure regulatory compliance and support with current standards and implementation of new standards (IPEC GMP/GDP, EXCiPACT, GDP etc). Collaborating within the Pharma Regulatory team on global business unit projects. Creation and management of product regulatory information in standardized format. Providing training on regula...