Chr. Hansen’s Human Health Business is looking for a Regulatory Specialist to support the registration process of our customers in Latin America (LATAM). Chr. Hansen is a market leader within probiotics for the dietary supplement and pharmaceutical industry. We are purely business to business but can take responsibility for the manufacturing process of our product up to the final consumer pack. The position is anchored in our Product Registration & Documentation function which is located in Denmark, Hoersholm, but the position may be based in Denmark, Hoersholm or Brazil (Valinhos or Sao Paulo area) depending on where we find the successful candidate. Your main responsibilities: • Manage Chr. Hansen’s overall registration support in the LATAM region. Create and maintain dossiers and files for registration and importation license in close collaboration with headquarters • Develop and maintain knowledge of LATAM registration requirements including emerging issues and communicate these requirements within the Human Health organization • Establish close liaison with the Human Health Regulatory Manager, Americas, who is responsible for External Affairs activities • Participate in internal and customer projects to provide regulatory guidance and facilitate establishment of regulatory documents for customer submissions. The responsibilities include assembling of registration files for customers in the LATAM region and assessing the impact of Chemistry, Manufacturing and Chemical changes on relevant regulatory submissions (especially “pharma like”) in the LATAM region.