RIF. 3635: REGULATORY AFFAIRS SPECIALIST
Our client is a Multinational Consumer Health Company
Role 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 & Skills
Relevant 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 English
Preferred
• 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