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Boston Scientific Regulatory Intern Bogotá 
Colombia, Cundinamarca 
402522446

Yesterday

Key Responsibilities

  • Support process optimization projects in the Regulatory Affairs area (e.g., database maintenance, regulatory controls, automation)
  • Assist in daily operations such as documentation consolidation and Invima dossier preparation
  • Collaborate on cross-functional projects with other departments
  • Conduct data analysis and prepare findings for reporting
  • Participate in process mapping to identify optimization and automation opportunities
  • Attend and contribute to team meetings

Required Qualifications

  • Currently pursuing a degree in Biomedical Engineering, Systems Engineering, Pharmaceutical Chemistry, Electronic Engineering, Mathematical Engineering, or a related field
  • Strong analytical and problem-solving skills
  • Excellent communication and teamwork abilities
  • Ability to clearly map and document processes and solutions

Preferred Qualifications (Nice to Have)

  • Skills in data cleaning and preprocessing to ensure accuracy and consistency
  • Interest or experience in programming languages, automation scripts, or database management
  • Familiarity with regulatory documentation and dossier assembly processes
  • Interest in regulatory affairs or process improvement initiatives