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Regulatory Affairs Specialist

Regulatory Affairs Specialist

EPM ScientificChazo, Galicia, España
Hace 14 horas
Descripción del trabajo

We're seeking a detail-oriented and proactive Senior Regulatory Associate to support the preparation and submission of high-quality regulatory documentation. This is a fantastic opportunity for professionals with 1-3 years of experience in Regulatory Affairs who are ready to take the next step in their career.

Key Responsibilities :

  • Publish, dispatch, and archive regulatory submissions in agency-recommended formats.
  • Ensure timely delivery of compliant, high-quality submissions aligned with client and internal standards.
  • Format, hyperlink, and process submission-ready documents using MS Word and Adobe Acrobat.
  • Troubleshoot technical issues related to document formatting and publishing tools.
  • Collaborate cross-functionally to plan, prepare, and perform quality control checks on submissions.
  • Support regulatory audits and compliance activities.
  • Maintain up-to-date knowledge of agency standards and submission procedures.
  • Manage technical aspects and provide status updates for assigned submissions.
  • Use publishing and validation tools effectively.
  • Mentor junior staff and contribute to SOPs, work instructions, and training materials.

What We're Looking For :

  • Experience : 3+ years in Regulatory Affairs within the pharmaceutical industry.
  • Strong knowledge of electronic submission standards and tools.
  • Proficiency in MS Word, Adobe Acrobat, and publishing / validation platforms.
  • Excellent communication and collaboration skills.
  • Ability to work independently and manage multiple priorities.
  • Crear una alerta de empleo para esta búsqueda

    Regulatory Specialist • Chazo, Galicia, España

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