Lyon-Based Regulatory

il y a 2 jours


Lyon, France Nemera Temps plein

A global manufacturer of drug delivery systems is seeking a Regulatory & Compliance Project Manager to lead regulatory projects in Lyon. This role involves collaboration with development teams, preparing regulatory documents, and ensuring compliance with industry standards. The ideal candidate will have an engineering degree, at least 5 years experience in the pharmaceutical or biomedical fields, and strong English skills. Join a fast-growing team dedicated to improving patients' lives with innovative solutions.
#J-18808-Ljbffr



  • 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 NonStop Consulting Temps plein

    Chemical Regulatory Manager – Lyon Our client, a leading global provider of market expansion services with a strong presence in the chemical industry, is seeking a skilled and dedicated Chemical Regulatory Manager. This pivotal role will be based at their offices on the periphery of Lyon, with a flexible hybrid model allowing for 2 days of home working per...

  • Entry Level

    il y a 2 semaines


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a **full-time, office-based** Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your, education,...

  • Entry Level

    il y a 2 jours


    Lyon, France Medpace, Inc. Temps plein

    Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...


  • Lyon, France Nemera Temps plein

    We are currently looking for passionate people ready to make a difference in the following open position: Regulatory Affairs Manager F/M/X, based in Lyon (7e). Within Nemera's headquarters, you will lead the Regulatory & Compliance design projects of drug delivery devices for one of our strategic products BU. You will report to the Quality and Regulatory...


  • Lyon, France Nemera Temps plein

    A leading medical device company in Lyon is looking for a passionate Regulatory Affairs Manager to lead regulatory and compliance projects across various business units. Key responsibilities include managing a team, developing regulatory strategies, and ensuring compliance with ISO standards. The ideal candidate has a Master’s degree and extensive...

  • Regulatory Affairs Manager MFX

    il y a 2 semaines


    Lyon, France Nemera Temps plein

    We are currently looking for passionate people ready to make a difference in the following open position: Regulatory Affairs Manager F / M / X based in Lyon (7e). Within Nemeras headquarters you will lead the Regulatory & Compliance design projects of drug delivery devices for one of our strategic products BU. You will report to the Quality and Regulatory...


  • 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...


  • Lyon, France Nemera Temps plein

    A global healthcare company in Lyon is seeking a Regulatory & Compliance Project Manager to ensure regulatory compliance of products. The role requires an engineering degree, 5+ years of experience in the pharmaceutical or biomedical industry, and strong project management and analytical skills. This position emphasizes collaboration with cross-functional...


  • 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...