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Starting Date: June
Duration: at least 6 months
In this role you have the opportunity to:
Support the Regulatory Affairs (RA) team for EU Medical Device Regulation (MDR) international in their daily tasks for product registrations and portfolio readiness.
You are responsible for:
Creating EU MDR trackers for products portfolio in international and keeping the documents updated
Ensuring group newsletter information collection is collected and dispatched on a monthly basis to the team
Manage properly well Regulatory requirements and databases to ensure time to market with clear and up to date regulatory information captured in the databases.
You are a part of:
RA international team and QnR international team based out of Eindhoven HTC
To succeed in this role, you should have the following skills and experience:
Currently studying Engineering, Medicine, Biotechnology, Chemistry, Law, Pharmacy
Experience or interest in Regulatory domain
Good working knowledge of Excel (must)
Organized and detail-oriented
Solution-oriented, problem-solving mindset
Ability to work independently and autonomously
Strong motivation to develop professionally
Good knowledge of English
In return, we offer you:
Work with passionate and insightful colleagues who share your drive to create a superior customer experience
Build your career in an international company that markets innovations that matter to you
Why should you join Philips?
Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum .
To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog . Once there, you can also learn about our recruitment process , or find answers to some of the frequently asked questions .
Notes
Required documents in order for us to continue with your application:
- Resume
Please note that in order to be considered for an internship, you need to be registered as a student during the entire internship period . Formal documentation of which may be requested at any time. Students from outside the EU need to fill in a NUFFIC agreement, which needs to be signed by the student and the university.
Please note that the contents of our regular internship assignments are not suitable for professionals (and/or MBA students) with professional work experience.
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