About Zuellig Pharma Zuellig Pharma (ZP) is one of the largest healthcare services groups in Asia and our purpose is to make healthcare more accessible. For over 100 years, we have been the trusted partner for healthcare companies looking to realize opportunities in Asian markets. With our deep-reaching infrastructure and sole focus on healthcare, we offer our clients unparalleled access to all healthcare channels across 13 countries in the region. Our focus is always about combining our market insight with a thorough understanding of your needs to deliver the best solution that connects you to patients. We believe delivering your products is only the first step to capturing the Asian markets. That is why we have continued to invest in developing innovative solutions that expand across Distribution, Clinical Reach, Sales & Marketing, Patient Centered Services, and Community Pharmacies. Zuellig Pharma is the leading provider of distribution services to manufacturers in the life science industry in the Asia Pacific region. With operations in 13 countries or territories Zuellig Pharma has strong market positions, critical mass, broad geographic coverage and significant potential for continuing growth. Purpose of the Role: The intern will support regulatory operations and compliance activities across multiple markets, assisting in the preparation and maintenance of documentation required for product registrations, variations, and regulatory submissions. What You'll Do : Assist in compiling, formatting, and reviewing regulatory submission documents (e.g., product registration dossiers, variation applications, renewals). Support labelling updates and packaging compliance checks in accordance with local regulatory requirements. Maintain regulatory tracking tools, databases, and documentation repositories. Perform regulatory intelligence activities, including monitoring updates from local authorities (e.g., NPRA, HSA, DRU). Assist in the preparation of regulatory reports and summaries for internal stakeholders. Coordinate with cross-functional teams (QA, Commercial, Supply Chain) to gather necessary documentation. Support administrative tasks including archiving, scanning, and organizing regulatory files. Performs other duties as assigned when required. What will make you successful: Must-Have: Bachelor in any science discipline preferably Pharmacy or Science Advantage to Have: Proactive with excellent communication skills Why Join Zuellig Pharma: We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success. We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly. As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region. Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities. Our Total Rewards program is designed to support your overall well-being in every aspect. Show more Show less