Philips Regulatory Affairs Student 

Israel, Haifa District, Haifa 

108340825

Regulatory Affairs Student

You are responsible for

• Compile and maintain regulatory documentation databases or systems
• Support cross functional teams with regulatory guidance
• Coordinate efforts associated with the preparation of regulatory documents or submissions
• Coordinate, prepare, or review regulatory submissions for domestic or international projects
• Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation

To succeed in this role, you’ll need a customer-first attitude and the following

• Student for M.Sc. in BiomedicalEngineering/ Life Sciences, orequivalent degree
• Grades – 80+
• At least 1.5 years left before graduation
• Ability to work at least 18 hours per week (not including Friday)
• Fluent in English
• Relevant experience and familiarity with medical device industry - an advantage

Our hybrid working model is defined in 3 ways:

The way we work and our workspaces are designed to support our well-being, offer career advancement opportunities, and enable us to be at our best.