Regulatory - Label Specialist (M/F)

il y a 2 semaines


Lyon, France FMC Temps plein

FMC Corporation is a leading specialty company focused on agricultural technologies. FMC provides innovative and cost-effective solutions to enhance crop yield and quality by controlling a broad spectrum of insects, weeds and disease, as well as in non-agricultural markets for pest control.

FMC is a globally diverse organization that offers its employees exciting opportunities to work on challenging projects that are important to the achievement of our strategic objectives. Your education and professional experience are valued and put to use from day one. Your success at completing key initiatives can result in a varied, progressive and fulfilling career with FMC.

With a corporate culture of innovation, integrity, responsibility and customer intimacy, we foster “The Right Chemistry” in everything we do. We are looking for people to join us in creating, developing, and improving our products, our processes, and our markets. If you are ready to make a difference every day, FMC is ready to talk to you.

**Poste**:
We are looking for a highly motivated individual with a basic knowledge of the regulatory process for plant protection products who is looking for the next step in their career.

**Responsibilities**:

- Responsible for the preparation/amendments/updates of labels (France, Great Britain, Ireland). Making sure that they are in compliance and avoiding delays in product supply.
- Responsible for the preparation/amendments/updates of MSDS (France, Great Britain, Ireland). Making sure that they are in compliance and avoiding delays in product supply.
- Maintaining Internal and external Regulatory database ((France, Great Britain, Ireland).
- Assisting with Poison center Notification (EU).
- Preparing and keeping product material up to date also with respect to stewardship; labels, website and SDS.
- Work closely with the EU country regulatory managers to update registration timelines the internal database
- Assisting in preparation and submission of dossiers/documents to the regulatory authorities

**Profil**:
3-5 years university preferably in a regulatory science or related discipline (Agriculture, chemistry, toxicology, eco-toxicology, biochemistry or environmental science).
- Basic knowledge of crop protection industry: technical, commercial, farming techniques, crop specific issues, etc. is preferred but not essential as training can be provided.
- Proactive and strong problem-solving ability with sound judgment and organizational skills.
- Able to work individually but also as part of a team in a highly dynamic environment.
- Fluency in written and spoken English



  • Lyon, France ResMed Inc Temps plein

    Regulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: Saint-Priest, Lyon, Francetime type: Full timeposted on: Posted Todayjob requisition id: JR\_046400**Contexte et objectifs du poste**Au sein de l’équipe Regulatory Affairs EMEA, vous jouerez un rôle clé dans la gestion de toutes les activités réglementaires...


  • Lyon, Auvergne-Rhône-Alpes, France Consult Temps plein

    Vous êtes minutieux/se, rigoureux/se et avez une expérience en gestion de la sécurité des produits chimiques ?Expérimenté(e) en coordination de documentation réglementaire ?Vous souhaitez faire partie d'une organisation leader dans le domaine chimique en matière d'innovation produit et d'efficacité opérationnelle ?Nous recrutons actuellement un(e)...

  • Chemical Regulatory

    il y a 1 semaine


    Lyon, France Envu Temps plein

    A global leader in environmental safety is seeking a Chemical Product Regulation & Safety Specialist in Lyon, France. The role includes establishing and managing the integrity of safety data, ensuring compliance with regulations, and supporting audits. Ideal candidates will have a relevant degree and over 5 years of experience in regulatory affairs. Strong...


  • Lyon, France Astek Temps plein

    A leading CRO solutions provider is recruiting a Senior Preclinical Biostatistician in Lyon, France. The role focuses on ensuring compliance with evolving IVDR regulations. Candidates should have a higher education in Life Sciences and 2-5 years of experience in regulatory affairs for medical devices or IVDs. Key responsibilities include preparing technical...

  • Regional Regulatory Manager

    il y a 6 heures


    Lyon, France FMC AGRO POLSKA SP. Z O.O. Temps plein

    **About us** We, FMC Agricultural Solutions, provide innovative crop protection solutions to growers around the world. Thanks to the commitment of our 5,200 employees, we are one of the six largest crop protection manufacturers in the world. For any FMC office located in EU we are looking for a **Regional Regulatory Manager (m/ f/ d)** As a Regional...


  • Lyon, France 425 ResMed SAS Temps plein

    Contexte et objectifs du poste Au sein de l’équipe Regulatory Affairs EMEA, vous jouerez un rôle clé dans la gestion de toutes les activités réglementaires relatives au dispositif médical sur mesure Narval CC, produit de classe I (MDR 2017/745) et autres services / produits associés. Poste à forte composante opérationnelle, il requiert une...


  • Lyon, Auvergne-Rhône-Alpes, France Resmed Temps plein

    Contexte et objectifs du posteAu sein de l'équipe Regulatory Affairs EMEA, vous jouerez un rôle clé dans la gestion de toutes les activités réglementaires relatives au dispositif médical sur mesure Narval CC, produit de classe I (MDR 2017/745) et autres services / produits associés. Poste à forte composante opérationnelle, il requiert une expertise...

  • Regulatory Affairs Officer

    il y a 1 semaine


    Lyon, France Astek Temps plein

    Regulatory Affairs Officer - Lyon, France (F/M)Join to apply for the Regulatory Affairs Officer - Lyon, France (F/M) role at Astek.About UsAlsinova, a subsidiary of the Astek Group, specializes in Life Sciences. We support pharmaceutical, biotech, and medtech companies with expertise in regulatory affairs, clinical development, data, quality, and...


  • Lyon, France Barrington James Temps plein

    A global leader in sports medicine is seeking a Clinical Affairs Specialist to contribute to regulatory and clinical activities. This role requires a biomedical engineer with at least 5 years of relevant experience in medical devices and expertise in regulatory documentation. You will be responsible for analyzing clinical literature, drafting Clinical...

  • Regulatory Affairs Officer F

    il y a 1 semaine


    Lyon, France Astek Temps plein

    Alsinova, the Astek Group subsidiary offering a complete CRO solution, is recruiting a Senior Preclinical Biostatistician for a project in the pharmaceutical sector. Your mission (should you decide to accept it) As a Regulatory Affairs Officer, you will contribute to ensuring that the company's IVD products remain compliant with the evolving IVDR regulations...