Tổng quan

• Mức lương

  12,000,000 VND ~ 20,000,000 VND

• Ngành

  Manufacturing(Pharmaceutical/MedicalEquipment)

• Mô tả công việc

  【Job Summary】
  - Responsible for managing and supervising the validity of legal documents related to medical devices in Vietnam, ensuring the organization’s compliance with applicable legal standards. Monitor legal updates, assess impacts, coordinate with regulatory agencies, and support internal compliance.
  - In addition, responsible for managing and updating standard-related documents for the company’s products.
  
  【Job description】
  1. Monitor legal trends:
  - Collect and analyze new or amended legal documents related to medical devices in Vietnam, including laws, decrees, circulars, and decisions.
  - Develop and update the legal document database.
  2. Assess standard impacts:
  - Assess how new legal documents affect business activities, product registration, and the company’s market access.
  - Summarize key points of standard changes and report to relevant departments.
  3. Support compliance and implementation:
  - Collaborate with departments such as QA/QC, R&D, and Production Management to ensure legal compliance.
  - Draft internal regulations and SOPs (Standard Operating Procedures) based on legal requirements.
  4. Check and report documents:
  - Accurately check and archive legal documents, licenses, and approval documents.
  5. Internal training and support:
  - Organize and conduct internal training on standard requirements.
  - Support legal risk assessment related to product registration, labeling, and market activities.
  
  【Company/Job Attraction】
  - Opportunity to learn and improve sales skill with international standards.
  - Full benefits package
  - The opportunity to work in a large corporation, nice background for future career path