Job Summary: Boehringer Ingelheim is seeking enthusiastic undergraduate or master’s students for its 2026 Internship Program, focused on Pharmaceutical Regulatory Affairs. Key Highlights: 1. Start your professional career in the Pharmaceutical Industry 2. Learn about regulatory processes in a dynamic environment 3. Develop key competencies in Regulatory Affairs Would you like to launch your professional career in the Pharmaceutical Industry and become part of our talent community? If you are in your final year of an undergraduate degree or pursuing a Master’s/Postgraduate program in fields such as Health Sciences, Engineering, Business Administration, Communications, Information Technology, or related disciplines—and are interested in starting your internship in April 2026—this is your opportunity! At Boehringer Ingelheim, we are launching the new edition of our 2026 Internship Program, aimed at individuals who are enthusiastic, eager to learn, and committed to our purpose: improving the lives of present and future generations. We are currently seeking candidates for the following two positions: **1\. RASC Regions CTA Submissions** The RASC Regions (Regulatory Affairs Service Centre) provides direct support to the Corporate Division and is organized into two main sections: one focused on product-related regulatory activities and another dedicated to overseeing Clinical Trial Application (CTA) submissions. During your internship, you will learn the processes required to prepare, submit, and maintain documentation necessary for clinical trial authorizations at the EU level. This experience will provide you with a comprehensive understanding of regulatory procedures within a dynamic and cross-functional environment, offering valuable insight into how regulatory affairs operate in the pharmaceutical sector. Thus, you will consolidate your technical knowledge and develop key competencies such as analytical ability, organizational skills, and methodological rigor. This experience will allow you to complement and deepen the knowledge acquired across various academic subjects and throughout your university studies. **What will your day-to-day look like?** * You will support the tracking and management of clinical trials submitted under the Clinical Trials Regulation. * You will participate in the submission of clinical trial applications alongside your mentor, collaborating with teams across multiple European countries. * You will provide specific support in notifying milestones and key dates related to clinical trials. You will contribute to maintaining and updating our Power BI dashboard, which consolidates data from all ongoing clinical trials within the company. * **2\. RASC CMC** The RASC-CMC department plays a key role within Regulatory Affairs, leading and coordinating globally scoped regulatory activities. Its mission focuses on ensuring the proper management and submission of variations, renewals, and new Marketing Authorisation Applications (MAAs), guaranteeing regulatory compliance and technical consistency across all markets. As part of its activities, the team fosters the development of essential regulatory competencies—including technical analysis, organization, strategic planning, and negotiation skills—promoting a collaborative environment oriented toward operational excellence. This position is embedded within this international setting, offering the opportunity to actively participate in core CMC regulatory processes and contribute to maintaining global product compliance. **What will your day-to-day look like?** * You will learn how to assist in preparing and compiling documentation required for Renewal submissions, working closely with the team. * You will collaborate in evaluating changes and support the preparation of documentation required for quality-related variations, gaining hands-on experience in CMC regulatory processes. * You will participate in preparing new MAAs, learning how to coordinate information and understand regulatory requirements for initial applications. * You will assist in managing queries from regulatory authorities and customers, learning how to gather technical information and support response preparation. **What kind of profile are we looking for?** * **Education:** Bachelor’s degree in Health Sciences (preferably Pharmacy) and a Master’s degree in Pharmaceutical Marketing or Pharmaceutical Industry—or equivalent. * **Competencies:** Proactivity, organization, flexibility, and enthusiasm, with the ability to collaborate effectively in a team. * **Languages:** Advanced level of English. * **Availability:** Start date on 24 April 2026, with the possibility of completing a 12-month internship agreement. **What do we offer?** Here are some examples of how we’ll support you: * Paid internships (€1,000/month – 40 hours/week). * A mentor to guide your learning journey. * An intern community offering activities to foster your development. * Campus in Sant Cugat del Vallès: outdoor spaces, smartworking options, cafeteria, transportation service (shuttle from FGC station). * Flexible working hours. * Continuous training: language courses, soft skills e-learning platform, LinkedIn Learning, and more. * Access to Wellhub. If you are interested in joining this new edition of our internship program and meet these requirements, don’t hesitate to apply!