17 ott - Italia
Cosmoderma
Cosmoderma Commerciale S.r.l. is a company specialized in the development and contract manufacturing of cosmetic products.
We are looking for a Regulatory Affairs Specialist to manage our Regulatory Affairs function and ensure the correct handling of technical and regulatory documentation for cosmetic products developed and manufactured for our clients.
The position will be based at our new operational office in the Meridiana district of Casalecchio di Reno , with regular interaction with the company's production site in San Benedetto Val di Sambro.
The selected candidate will initially work alongside the current Regulatory Affairs Manager, gradually becoming the main point of reference for regulatory matters within the company. The role will involve close collaboration with R&D;, Sales, Graphic Design, Quality and Production teams, supporting product development projects from the formulation stage through to market launch.
Main Responsabilities Management of the Regulatory Affairs function
Preparation, review and management of regulatory documentation for cosmetic products
Management and verification of Product Information Files (PIF)
Support with CPNP notifications
Review of claims, labels, artworks and product texts from a regulatory perspective
Collection and verification of technical documentation relating to raw materials, packaging and finished products
Communication with clients, external laboratories, consultants and safety assessors
Regulatory support for products intended for EU and non-EU markets
Support to the Quality Management System in relation to audits, procedures and regulatory documentation
Coordination of regulatory priorities in collaboration with the other company departments
Required qualifications and skills Degree in a scientific field, preferably Chemistry, Pharmaceutical Chemistry and Technology, Pharmacy, Biotechnology or a related discipline
Knowledge of Regulation (EC) No. 1223/2009 on cosmetic products
Knowledge of cosmetic technical d
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