Challenging position for the real go-getter within for a large international pharmaceutical company. Job Description We are looking for an experienced person to fill this challenging all-round position. Focus areas will be Regulatory Submissions, Labeling and Artwork, coordination of , , and , and much more. The duration of this position initially is months. for new and authorized pharmaceutical product through timely preparation for submission of variations, renewal applications, PSURs and any other necessary application/notification. Responsible for correct/complete intake of the documents and procedure that trigger initiation of introductions / changes. Collecting all necessary information for preparation of new product labeling, such as technical specifications, design specifications, registration requirements and texts. Reviewing , and as well as coordination of Module improvements ( or other programs). Contact person for internal and external stakeholders such as, Packaging sites, External artwork center, Regulatory entities, , Regulatory- and -departments. Requirements Bachelor degree in a life science related field. Excellent communication skills (fluent in English) as well as organization and planning. Senior level working experience in a fast paced environment with high volumes of work within RA or related field. You are focused, determined, problem solving, and business keen. You have a valid work permit for . Benefits Contract months via . Salary € - € gross monthly based on hours. Working hours - hours. Region Oss. Vacancy number .