This internship offers an excellent opportunity to gain hands-on experience in the medical device regulatory landscape within a leading global healthcare company
Job Summary
This internship offers an excellent opportunity to gain hands-on experience in the medical device regulatory landscape within a leading global healthcare company.
The role involves assisting the Regulatory Affairs team in preparing and submitting regulatory documents to health authorities across Latin America and supporting various regulatory projects.
GE Healthcare fosters an inclusive culture emphasizing humility, transparency, focus, ownership, and integrity while providing competitive compensation and professional growth opportunities.
Matching Summary
This internship offers an excellent opportunity to gain hands-on experience in the medical device regulatory landscape within a leading global healthcare company.
Skills & Requirements
Must-have
Preparation of regulatory documents
Regulatory database maintenance
Multifunctional team collaboration
Regulatory compliance review
Microsoft Office Suite proficiency
Strong organizational skills
Nice-to-have
High level of English proficiency
Interest in medical device industry
Ability to work independently and in teams
Excellent written and verbal communication
Attention to detail
Key Requirements
Undergraduate student from 7th semester onwards
Fields: Industrial Engineering, Systems Engineering, Data Analysis, Chemistry, Pharmaceutical Chemistry, Pharmacy, Biomedical Engineering, Life Sciences
Availability Monday to Friday 8:00 am to 5:00 pm
Strong academic performance
Bilingual Spanish and English communication skills