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