Basel is the headquarters of the Roche Group and one of its most important centres of pharmaceutical research. Over 8,500 people from approximately 90 countries work in Basel, which is one of Roche`s largest sites.
As an Intern within the Pharma Technical Regulatory Affairs Group in Basel, you will gain insight into the work of Technical Regulatory Affairs professionals who are responsible for providing the Regulatory input and leadership for quality-related aspects of pharmaceuticals. The activities span the whole lifecycle of the product, from clinical trials all the way to the maintenance of products at the end of their lifecycle.
During the internship you will:
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
To take on this challenging opportunity you are enrolled in a Master’s or Ph.D. program in life sciences or pharmaceutical sciences nearing the end of your studies.
Your qualifications include but are not limited to the following:
Please apply with your CV and cover letter by the 'apply' button below
Remember - you found this opportunity on Qreer.com
Education Backgrounds: |
Biomedical Science Environmental Engineering Healthcare Science |
Specialties: |
Life sciences Pharmaceutics Project Management Quality Engineering Research (R&D) |
Education Level: |
Postgraduate (Masters) Doctorate (PH.D) |
Experience: |
0 - 2 years 2 - 5 years 5 - 10 Years |
Languages spoken: |
English |
Job Location: | Basel , Switzerland |
Type: Job
Deadline: 30th May 2017
Job reference (ID): 11578
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