About Us
With over 185 years of history, we are a leading health and wellness company. Our portfolio includes iconic brands such as Aquilea, Fisiocrem, Laborest, Sidroga, Biodramina, Aerored, Fave de Fuca, Halibut, Ems, and Depuralina, with a strong presence across major European markets.
We believe in the power of nature, enhanced by science, as the best way to improve human health and wellbeing sustainably. Our goal is to create a positive impact on both people's lives and the planet.
We are currently seeking a highly motivated and skilled accounts payable who would be responsible for processing invoices, ensuring accurate and timely payments, and maintaining strong relationships with vendors and internal stakeholders in both France and other regions.
Be prepared to:
* Support for new projects in collaboration with R&D, Marketing and Project Management
* Review of possible claims and communication opportunities for new projects or products already in the market
* Establish synergies between the different local regulatories with a global approach for the development of any new project.
* Ensure regulatory compliance of all the products (ingredients permitted, allowed quantities, etc...) in local and global formulations.
* Control and adaptation to new regulations.
* Preparation of packaging texts, review of proposal and approval of final artworks.
* Coordinate between the different local regulatories for the multilingual packaging project.
* Supervision and/or preparation PIF, TD, eCTD dossiers. Life cycle maintenance of these dossiers.
* Registration and notifications tasks of different products (food supplements, cosmetics, medical devices or OTCs) prior to its commercialization.
* Request of different national codes required for commercialization.
* Verification of the communication of marketing materials, websites, etc...
* Direct contact with Regulatory bodies and consultants.
* Direct contact with RoW partners to provide all the information and documents necessary for registration of products abroad.
* Post-market surveillance activities for medical devices. Coordinate with PV department for OTCs and medical devices.
* Management of information (databases, SOPs...) according applicable ISO requirements (22000, 14001, 13485...)
Sector:
Función:
For this role we require:
* University degree in Life Sciences (Pharmacy, Biology, Chemistry or related fields); postgraduate studies in Regulatory Affairs are a strong asset.
* 2-6 years of experience in Regulatory Affairs within the food supplements, cosmetics, medical devices or over the counter (OTC) sectors.
* Solid understanding of EU and international regulatory frameworks, including requirements for ingredients, claims, labelling and product registration.
* Strong communication, organizational and analytical skills, with the ability to manage multiple projects, documentation and deadlines in a structured manner.
* High level of French, Spanish and English.