Are you studying full-time in the healthcare sector and/or do you enjoy working with English-language specialist literature from the scientific / medical field as part of your studies? Then join our Regulatory Writing Team as of now and gain your first practical experience in an international healthcare company! Here you will gain insights into the preparation of clinical approval dossiers and the associated evaluation of clinical studies, published study results and treatment guidelines for parenteral nutrition products. You will also learn how to deal professionally with literature and references. During your work, you will be trained in the use of reference management software and in PDF editing at expert level. You will also be supported by an experienced team of experts and trained in regulatory processes. In this way, you can get a taste of practical experience, make contacts, explore possible career paths - and fill your study fund at the same time. You will order copyrights (e.g., medical literature, international treatment guidelines) and maintain the literature pool You will also be responsible for maintaining and creating the database using EndNote software You will be responsible for formatting and editing PDF documents using Toolbox software Even more: you will provide support in the regulatory, electronic document management system and in the quality control of regulatory documents