Hochschulpraktikum
Hochschulpraktikum
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:
- Support Technical Regulatory Managers in their daily tasks and gradually assume responsibility for agreed individual projects
- Get hands on experience by working on various quality-related regulatory activities across the whole development value chain from clinical trial applications through to license applications and maintenance
- The project you will work on is real and you will be generating genuine added value
Further take away opportunities:
- Many learning and training opportunities that will help improve your personal development
- Learn to work in a global company, to network and to collaborate with stakeholder groups
- Be a member of our Interns Network and get to experience the culture of Basel in the heart of Europe
Your Profile
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:
- First regulatory experience or knowledge in regulatory affairs
- Ability to drive activities, work under pressure and to tight timelines
- Good coordination and excellent communication skills
- Strong organizational and analytical skills
- Outstanding motivation and willingness to learn
- Excellent English language skills
Applications need to include a CV, a motivation letter and your answer to these 3 questions:
- Why do you want to do an internship in Technical Regulatory Affairs?
- What relevant skills and experience will you bring to this position?
- What challenges do you see in the field of Technical Regulatory Affairs?
The preferred start date of the internship is beginning of September 2019.
Due to regulations non-EU/EFTA citizens have to provide a certificate from the university stating that an internship is mandatory as part of the application documents.
The preferred start date of the internship is beginning of September 2019.
Due to regulations non-EU/EFTA citizens must provide a certificate from the university stating that an internship is mandatory as part of the application documents.
Wer wir sind
At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche is an equal opportunity employer.
Job-Fakten
- Standort Switzerland, Basel-City, Basel
- Funktion Vocational & Development Programs
- Subfunktion Internship
- Arbeitszeit Full time
- Funktionsebene Entry Level
- Art der Anstellung Temporary (Fixed Term)
- Firma/ Division Roche Pharmaceuticals
- Posted since 2019/07/22
- Job-ID 201901-100798
Kontaktieren Sie uns
Mrs. Nicole Mohler