Regulatory Affairs Specialist
Pubblicato il 22-08-2026 - Chromavis in Offanengo
**Technical Skills** The Finished Products Regulatory Affairs Specialist ensures the creation and administrative monitoring of all documents necessary for the company to comply with current cosmetic laws and regulations: - Perform regulatory checks following Customers Banlist and international regulations regarding customers and internal briefs and requests
- Prepare Margins of Safety (MOS) request and submit them to the safety assessor
- Select external laboratories following liability, prices and delays in order to quote and organize safety and efficacy testings respecting product categories and claims.
- Plan, organize, gather and spread safety and efficacy testing results while helping interpretation of them
- Check finished products labelling regarding the regulation in force
- Gather all documents for CPSR requests and ask for CPSR
- Register CPNP notifications where relevant
- Gather all data and documents needed in the Product Information File, OTC reports and specifications for sending to the customers and archive them
- Update CPSR, MOS, PIF/OTC reports and Specifications for existing products following the regulations in force in the case of change controls
- Follow new developments, answering to customers requests or local authorities and gathering complementary data if necessary
- Be regulatory support for customer’s registrations and legalizations
- Ensure Regulatory,
scientific and technologic watch for Europe and International countries
- Manage regulatory watch on going topics when necessary
- Can participate to webinars, Regulatory exhibitions
- Participate in building and maintenance of regulatory database. Ensure that the data
- entered is accurate and justified to improve data centralization **Project Management**
- Follow all the steps of formula development in order to give regulatory support when needed to R&D; laboratory, Sales Marketing and Project Managers.
- Respect leadtimes of development planning
- Prepare and submit the technical agreement to the Project Managers to define RACI linked to the development **Hard Skills**
- Background: Master in science with experience in Cosmetic Regulatory
- SOP & IT tools expertise (ORACLE, COPTIS, Pack Office )
- REGULATORY EXPERTISE (European and International regulatory, safety and efficacy testings)
- PROJECT DATA MANAGEMENT (RM, formula, packaging, testings )
- Language: ENGLISH with professional use
- TOXICOLOGICAL KNOWLEDGE **Soft Skills**
- Rigor/Attention to detail, Adaptability, Collaboration, Organization, Communication, Customer
- service, Lean oriented, Team spirit joinus Contratto di lavoro: Tempo pieno, Tempo indeterminato, Apprendistato Retribuzione: €24.653,45 - €32.000,84 all'anno Vantaggi: - Buoni pasto
- Orario flessibile Sede di lavoro: Di persona