Regulatory Affairs Graduate Intern
Riyadh, Saudi Arabia
Hiring Manager: [[hiringManagerName]]
Recruiter: Ines Somorai
Regulatory Affairs Graduate Intern
At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world.
At Boston Scientific you can take the first step towards a meaningful career by joining a passionate team and contributing to improve the health of people around the world. You’ll have the opportunity to grow and nurture your talent in an inclusive and innovative environment.
Choosing the right place to work is an important decision. Read all the details below and if it sounds like you, consider joining the team.
This role is a 12-month contract, starting in July 2025 and is based Riyadh office.
Successful candidates may be retained by Boston Scientific at the end of the contract.
About the Role:
In your role you will working for a great local team supporting the Regulatory affairs team. You will be involved in product market access related projects, learning about regulatory environment and changes that are or will impact on Boston Scientifics medical devices.
KEY RESPONSIBILITIES:
- Assist in preparing and submitting regulatory submissions
- Support updates to Technical Documentation to align with EU Medical Device Regulation (MDR)
- Help improve regulatory processes, including database maintenance, automation, and regulatory controls
- Work with different departments to ensure compliance
- Conduct data collection, analysis, and interpretation to support regulatory decision
PROFILE REQUIREMENTS
- Pursuing a degree in Science or Healthcare-related fields, such as Engineering, Legal, Communication, Master’s degree in Regulatory, Clinical Affairs, or Public Health
Skills & Experience:
- Excellent written and verbal communication skills.
- Basic understanding of data collection, analysis, and interpretation.
- Strong computer skills, including word processing, PowerPoint, and database management.
- Ability to translate technical information into clear documentation.
- Quick learner, self-motivated, and able to work independently.
Requisition ID: 606694
Job Segment:
Regulatory Affairs, Medical Device, Compliance, Public Health, Law, Legal, Healthcare