Regulatory Affairs Specialist: FDA Submissions

hace 4 días


Barcelona, España ESTEVE A tiempo completo

A pharmaceutical company in Barcelona is seeking a Regulatory Affairs Specialist to manage the regulatory lifecycle of US FDA-approved products. The role includes preparing FDA documentation, maintaining compliance, and collaborating with cross-functional teams. Candidates should have a Bachelor's degree in a relevant field and 3–5 years of experience in Regulatory Affairs, along with fluency in English and Spanish. This full-time position offers a mid-senior level opportunity in a dynamic environment.#J-18808-Ljbffr



  • Barcelona, España ESTEVE A tiempo completo

    Job description: 1. FUNCTIONAL CONTENT Main Role The Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products, ensuring ongoing compliance and supporting regulatory activities for the ongoing new product development projects. This role requires close collaboration with cross-functional teams...


  • Barcelona, Barcelona, España ESTEVE A tiempo completo

    Job description:1. FUNCTIONAL CONTENTMain RoleThe Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products, ensuring ongoing compliance and supporting regulatory activities for the ongoing new product development projects.This role requires close collaboration with cross-functional teams including...


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