Workplace type
Hybrid
About The Position
Assist in preparing, creation and maintenance regulatory documentation for FDA and CE submissions.
Flexible working hours to accommodate academic schedules.
Opportunity to gain hands-on experience in the medical device regulatory field.
Requirements
Currently pursuing a Bachelor's degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.
Interest in Regulatory Affairs is preferred.
Any internship or coursework related to medical devices or regulatory affairs is an advantage.
Highly motivated and Coachable.
Strong attention to detail and organizational skills.
Excellent English and Hebrew.
Ability to work independently and as part of a team.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).