
Job Description
Your role is to be responsible for the regulatory affairs activities in Estonia, preparation and filing of Regulatory submissions for all company’s new and existing products registered in Estonia.
Requirements
We expect you to have previous experience in monitoring of local regulatory requirements, knowledge of local registration requirements, a higher education in Life sciences and an interest in pharmacology. You consider analyzing data and attention to detail as your strengths. You speak both Estonian and English at a very good level.
Company offers
We offer the chance to be a part of a change for the better, to share your ideas and help create a new and a strong foundation for the company and its processes. There is no worked out bonus system to present, but the company is open for discussion.