The Regulatory Affairs Intern will be responsible for providing support to deliver the regulatory strategy for assigned projects of Healthcare portfolio.
Here below some responsibilities:
- Maintaining and processing of local regulatory databases and systems, archiving of regulatory documents and management of electronic directories.
- Monitoring of Regulatory websites in order to detect law changes and new competitors.
- Support in the lifecycle management of medicines (variations, renewals, etc.)
and medical devices and in the preparation of documents to be submitted to Authorities.
Skills for the role
- Master degree in Chemistry or Pharmaceuticals
- Good level of English
- Proactivity, learning on the job attitude, working in team attitude, responsibility
**You'll succeed because**
you're curious by nature and an original thinker.
You've a strong academic background and an understanding of the product development process.
You're ambitious and motivated, hungry to take on responsibility in an entrepreneurial and dynamic environment.
You're also action-oriented, a pragmatic problem solver and share our drive to succeed.
Even when faced with obstacles.
**You'll love it because**
you'll get to make an impact like never before.
You'll be responsible for your own projects - we can't wait hear to your ideas.
The products you help us get out there will make people's lives better.
Our iconic brands will provide an incredible platform for you.
And our dynamic, ownership-driven culture will help bring the very best out of you, every day.
**Equality**:
All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.