
International Scientific Regulatory Affairs Specialist H/F - Adisseo
- Antony - 92
- CDI
- Adisseo
Les missions du poste
Overview
Welcome diversity and apply as you are !
At Adisseo, we cherish the value of diversity whatever IT may BE.
By joining Adisseo, you will join committed people who make the difference every day to contribute to this challenge.
By joining Adisseo, you will integrate a dynamic international environment.
By joining Adisseo, you will discover a world full of opportunities for every stage of your career by being actor to your professional journey.
Responsibilities
We are looking for an experienced professional to join our Scientific & Regulatory Affairs team, providing key regulatory expertise to drive growth and product launches.
- Mission
- Manage product approval in the countries and regions where the company operates (US, EU, CAN, CN) :
- Coordinate the generation of data required for building homologation dossiers by collaborating with cross-functional teams (primarily R&D).
- Co-develop and validate protocols, reports, and articles to BE included in the homologation dossiers.
- Draft regulatory dossiers and ensure proper submission in line with EU feed additive regulations, using EFSA and EU Commission tools correctly; and corresponding regulations as applicable.
- Follow up on the dossier approval process, including direct communication with the relevant authorities.
- Regulatory assessments of ingredients and scientific topics, including risk assessment reports with potential impact on Adisseo's business.
- Support other internal departments by providing regulatory advice (supporting and proofreading documents, answering customer inquiries, etc.).
- Regulatory and legal monitoring of new regulations and guidelines applicable to the company's products.
- Develop relationships with regulatory authorities and participate in industry associations to understand the regulatory environment and contribute to the drafting of relevant norms and legislation.
- Reporting, Relations & Contributions
- Reporting to the Scientific & Regulatory Affairs Manager.
- Ensure compliance with commitments related to authorizations (timing, costs and quality of the dossiers).
- Participate in product committees (development, launch).
- Provide support to entities and actively contribute to projects.
- Internal Relations : Collaborate with all services at the headquarters (marketing, business), industrial sites, commercial regions, including members of the regulatory network and customer service teams. Special relationship with Corporate R&D.
- External Relations : Mainly with regulatory authorities, industry associations, and consultants (toxicologists, nutritionists), as well as researchers (CRO).
- Required Skills
- Ability to work effectively in complex environments, results-driven, and with a strong regulatory compliance focus.
- Autonomous, leadership skills, excellent communication and persuasion abilities, team-oriented, and enthusiastic.
- Knowledge of applicable regulatory and legal standards (animal feed industry), with a minimum of 5 years of experience in dossier submissions in those jurisdictions
- Scientific background (Agriculture, Veterinary, MSc).
- Knowledge in human or animal nutrition.
- Fluent in English.