Regulatory Affairs

Q & RA department in Uppsala is now looking for a Regulatory Affairs (RA) to support our international growth.. The company work with everything from developing new products to production and distribution. Your main duties are to create registration applications for new and changed products, and to support our international regulatory affairs people on the various markets with information needed to enable their local submissions. Our RA is also involved in the creation of product-related information, such as instructions for use, and promotion material. You will also monitor the regulatory requirements on selected markets and provide regulatory input to[ the organization. You will communicate internally with R&D and Operations, and externally with the relevant authorities and international RA staff. As RA, you will be working in a creative environment with weekly international contacts. Qualifications: * University degree or equivalent required * 3+ years regulatory experience in medical device industry or equivalent * Knowledge of international regulatory requirements * Solid communication and interpersonal skills