Descrizione della posizione:
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
Please send your CV in English