Medical & Regulatory Affairs Junior Manager

Coordination, preparation and review regulatory submissions for national and European procedures, Ensure compliance with regulatory standards and guidelines, Interaction with regulatory agencies to expedite approval of pending registrations, Management and control of regulatory documentation, ensuring completeness, accuracy and proper archiving, Coordination the preparation of documents required for regulatory submissions and responses to authorities questions, Review labelling and promotional material for compliance with regulations, Work closely with other departments to ensure that compliance is maintained throughout the company, Develops/reviews country-specific labelling content for food supplements, cosmetics, medical devices and biocidal products, Participates in meetings and other project related meetings according to the company needs, Support Regulatory Country Intelligence activities, Maintenance of regulatory database and tracking systems. Bachelor's degree in Life Sciences (Pharmacy, Chemistry, Biology, Biochemistry or related discipline), Minimum of 4 years in Regulatory Affairs within pharmaceutical industry (focusing not only on medicinal products but also medical devices, cosmetics and food supplements), Familiarity with pharmacovigilance regulations is advantageous, Good understanding of regulatory frameworks and submission processes, including national and European regulations, Strong communication skills, both verbal and written, Strong attention to details and good organizational skills, Fluent in English, both written and spoken, Demonstrated team spirit and ability to work in matrix environment