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 documentation in depth and apply sound technical judgement when making decisions.

• Work closely with Project Managers, R&D, Quality, Marketing, Key Account Management, Procurement, Packaging, Design and Supply Chain teams.

• Ensure that new products are developed and launched in accordance with all applicable regulatory requirements.

• Contribute to the development of a growing Regulatory Affairs structure within an international and cross-functional environment.

What we are looking for:

• University degree in Pharmacy, Chemistry, Biotechnology, Toxicology or a related discipline.

• Solid and up-to-date knowledge of European cosmetic regulations.

• Previous experience in Cosmetic Regulatory Affairs (+ 5 years).

• Experience managing regulatory projects, coordinating cross-functional teams and stakeholders, working with external consultants and specialised technical providers.

• Knowledge of cosmetic safety assessment and toxicological documentation.

• Languages: Native or professional command of Italian and English (interview will be conducted in english). Spanish would be considered an advantage.

Nice to have:

• Master’s degree or postgraduate qualification in Regulatory Affairs, Toxicology, Cosmetic Safety or a related field.

• Knowledge of non-European cosmetic regulations.

What they offer:

• Opportunity to join an international and growing company within the cosmetics sector.

• Flexible starting time .

• Monday-to-Friday schedule.

• On-site working model (no hybrid or smart working option)