F. Hoffmann-La Roche AG
Student Internship in Technical Regulatory Affairs(m/w/x)
Full-timeInternshipOn-site
Basel
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NONovartis Pharma AG
Regulatory Affairs Postgraduate Program(m/w/x)
Basel
Full-timeOn-siteJunior
Nejo AI Summary
Global regulatory input and dossier preparation for pharmaceutical submissions. Master's or Doctoral qualification with a career interest in Regulatory Affairs required. Reasonable accommodation for disability, diversity and inclusion commitment.
Requirements
- Interest in Regulatory Affairs and pharmaceutical industry
- Career in Regulatory Affairs after Master’s or Doctoral qualification
- Collaborative mindset and task ownership
- Adaptability to different teams and concepts
- Excellent problem-solving skills
- Work and gain experience in cross-functional team
- Experience in multicultural and diverse environment
- Strong interest in Regulatory Affairs and Drug Development
- MSc, PhD or PharmD in Pharmaceutical Sciences/Pharmacy/Life Sciences or equivalent completion within last 24 months
- Fluency in English (written and spoken)
- CV and Cover letter in English required to apply
- Open minded with an international outlook
- Strong interpersonal skills and ability to communicate well
- Communication with people from various backgrounds/cultures
- Communication at different hierarchical levels
- Eligibility to work in Switzerland or studies completed at Swiss University
Tasks
- Interact with global project teams for regulatory input
- Support strategic development and submission planning
- Prepare high-quality dossiers for global regulatory submissions
- Support drug substance and drug product quality documentation
- Ensure compliance with regulatory requirements and guidelines
- Facilitate timely submission of variations and change control
- Develop and maintain globally consistent product information
- Analyze the EU Regulatory Framework for the RA community
- Monitor and evaluate legislation and guidelines from various sources
Education
- Compulsory education
Languages
- English – Fluent
Benefits
Other Benefits
- Reasonable accommodation for disability
Informal Culture
- Diversity and inclusion commitment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharma AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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NONovartis Pharma AG
Regulatory Affairs Postgraduate Program(m/w/x)
Basel
Full-timeOn-siteJunior
Nejo AI Summary
Global regulatory input and dossier preparation for pharmaceutical submissions. Master's or Doctoral qualification with a career interest in Regulatory Affairs required. Reasonable accommodation for disability, diversity and inclusion commitment.
Requirements
- Interest in Regulatory Affairs and pharmaceutical industry
- Career in Regulatory Affairs after Master’s or Doctoral qualification
- Collaborative mindset and task ownership
- Adaptability to different teams and concepts
- Excellent problem-solving skills
- Work and gain experience in cross-functional team
- Experience in multicultural and diverse environment
- Strong interest in Regulatory Affairs and Drug Development
- MSc, PhD or PharmD in Pharmaceutical Sciences/Pharmacy/Life Sciences or equivalent completion within last 24 months
- Fluency in English (written and spoken)
- CV and Cover letter in English required to apply
- Open minded with an international outlook
- Strong interpersonal skills and ability to communicate well
- Communication with people from various backgrounds/cultures
- Communication at different hierarchical levels
- Eligibility to work in Switzerland or studies completed at Swiss University
Tasks
- Interact with global project teams for regulatory input
- Support strategic development and submission planning
- Prepare high-quality dossiers for global regulatory submissions
- Support drug substance and drug product quality documentation
- Ensure compliance with regulatory requirements and guidelines
- Facilitate timely submission of variations and change control
- Develop and maintain globally consistent product information
- Analyze the EU Regulatory Framework for the RA community
- Monitor and evaluate legislation and guidelines from various sources
Education
- Compulsory education
Languages
- English – Fluent
Benefits
Other Benefits
- Reasonable accommodation for disability
Informal Culture
- Diversity and inclusion commitment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharma AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Pharma AG
Industry
Pharmaceuticals
Description
Das Unternehmen setzt sich für Vielfalt, Chancengleichheit und Inklusion ein und fördert innovative Lösungen zur Verbesserung der Patientenversorgung.
Not a perfect match?
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