Our client is a Multinational Consumer Health CompanyRole responsabilities:
Manage preparation of new regulatory documents, dossiers and applications to enable products to be launched and maintained in market;
Support key processes related to CMC, quality, labelling, artworks and local regulations.
Support the development of the strongest claims/advertising and promotion possible within the regulations, obtaining the required authorization;
Maintain required regulatory compliance databases, systems and processes.Qualifications SkillsRelevant previous experience of at least 3 years in a pharmaceutical/healthcare company
Good knowledge of pharmaceutical, laws and regulation and fluent management of the life cycle management
Knowledge of the fundamentals of medical devices
Scientific Degree (Pharmacy, Pharmaceutical chemistry, Chemistry or related disciplines) and Master in Regulatory Affairs is preferred
Fluent in EnglishPreferred
Good team player, with strong interpersonal skills to work well in cross-functional teams.
Works with a spirit of continuous improvement and innovation, creatively open to new ideas and methods.
Results-driven mindset and problem-solving skills.
Ability to work in a fast-paced, dynamic environment, managing multiple priorities.Location : Milan