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Student Internship in Technical Regulatory Affairs(m/w/x)
Producing high-quality CMC dossiers in an agile, digital environment. Prior regulatory affairs knowledge needed. Hands-on experience in global pharma, with interns' network membership.
Requirements
- Enrolled in life sciences or pharmaceutical sciences Master's, or graduated after 09/01/2025
- Prior experience or knowledge in regulatory affairs
- Ability to drive activities and work under time pressure
- Good coordination and communication skills
- Strong organizational and analytical skills
- Proficient English language skills
- Non-EU/non-EFTA citizens require specific enrollment and university certificates
Tasks
- Support regulatory professionals in developing innovative strategies
- Produce high-quality CMC dossiers in an agile and digital environment
- Operate as a member of global, self-managed squad teams
- Align with the organization's agile implementation
- Gain experience in quality-related regulatory activities
- Work on regulatory activities across the development lifecycle
- Contribute to operational and business excellence in regulatory affairs
- Manage regulatory documents
- Generate data and insights for regulatory advancement
- Utilize business systems to advance digital and data solutions
- Work on impactful projects
- Assist teams with daily tasks
- Take ownership of defined individual projects
Education
- Currently in higher educationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Other Benefits
- Hands-on experience in Technical Regulatory Affairs
- Global pharma insight
Learning & Development
- Develop regulatory expertise
- Learning and training opportunities
Mentorship & Coaching
- Interns' Network membership
Team Events
- Cultural immersion in Basel
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Student Internship in Technical Regulatory Affairs(m/w/x)
Producing high-quality CMC dossiers in an agile, digital environment. Prior regulatory affairs knowledge needed. Hands-on experience in global pharma, with interns' network membership.
Requirements
- Enrolled in life sciences or pharmaceutical sciences Master's, or graduated after 09/01/2025
- Prior experience or knowledge in regulatory affairs
- Ability to drive activities and work under time pressure
- Good coordination and communication skills
- Strong organizational and analytical skills
- Proficient English language skills
- Non-EU/non-EFTA citizens require specific enrollment and university certificates
Tasks
- Support regulatory professionals in developing innovative strategies
- Produce high-quality CMC dossiers in an agile and digital environment
- Operate as a member of global, self-managed squad teams
- Align with the organization's agile implementation
- Gain experience in quality-related regulatory activities
- Work on regulatory activities across the development lifecycle
- Contribute to operational and business excellence in regulatory affairs
- Manage regulatory documents
- Generate data and insights for regulatory advancement
- Utilize business systems to advance digital and data solutions
- Work on impactful projects
- Assist teams with daily tasks
- Take ownership of defined individual projects
Education
- Currently in higher educationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Other Benefits
- Hands-on experience in Technical Regulatory Affairs
- Global pharma insight
Learning & Development
- Develop regulatory expertise
- Learning and training opportunities
Mentorship & Coaching
- Interns' Network membership
Team Events
- Cultural immersion in Basel
About the Company
F. Hoffmann-La Roche AG
Industry
Healthcare
Description
Das Unternehmen ist ein führender Anbieter von pharmazeutischen Wirkstoffen und setzt sich für die Gesundheitsversorgung weltweit ein.
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