22 set - Milano
Bo Growth
Our client:
Our client is an international company within the beauty industry, specialised in the development and manufacturing of innovative cosmetic solutions for leading market brands.
Role misson:
Reporting to the Regulatory Affairs leaders, the selected person will lead and coordinate regulatory and toxicological assessment activities for cosmetic products, ensuring compliance with the legislation applicable in all markets where the company operates.
The Regulatory Specialist will also coordinate external consultants and specialised providers, ensuring the efficient execution of regulatory projects, the quality of the technical documentation and compliance with deadlines and business priorities.
Key responsabilities:
- Ensure compliance with current cosmetic legislation, particularly Regulation (EC) No 1223/2009, as well as other applicable international regulations.
- Coordinate the preparation, review and maintenance of regulatory dossiers and Product Information Files (PIFs).
- Oversee product safety assessments and the corresponding toxicological documentation.
- Technically review and supervise safety dossiers and toxicological documentation prepared by external specialists.
- Manage regulatory notifications and product registrations in the relevant markets.
- Monitor legislative and regulatory developments and assess their potential impact on the company's product portfolio.
- Act as a key point of contact with competent authorities, industry associations and regulatory bodies.
- Coordinate and support the development of Regulatory Affairs and Toxicology activities within the team.
- Define priorities, allocate resources and monitor compliance with deadlines and objectives.
- Select, appoint and manage external consultancy firms specialising in regulatory affairs, toxicology, claims, product safety and other technical areas.
- Manage budgets associated with regulatory projects and external professional services.
- Analyse technical and regulatory doc
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