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Quality Biosimilars Advanced Studies Masters-level Internship(m/w/x)
Building a digital database for Innovation & Development at a global healthcare leader, ensuring Quality System compliance. Master’s student in Biotechnology, Pharmacy, Bioengineering, or related field required. Mentorship from experienced leaders, clear pathway to future roles.
Requirements
- Master’s student in Biotechnology, Pharmacy, Bioengineering, Quality Management, Life Sciences, or related field
- Strong analytical mindset and interest in Quality, regulatory pathways, and biosimilar development
- Ability to transform complex information into structured, digital solutions
- Self-driven, detail-oriented, and comfort with global collaboration
- Curiosity, initiative, and ambition for high-impact projects
Tasks
- Build a digital database for Innovation & Development
- Capture QA project data and lead assignments
- Support Quality System transition and maintenance
- Ensure Quality System compliance
- Ensure documentation readiness
- Define and implement standardized Change Control for biosimilars
- Develop Quality SharePoint for Change Control
- Create Change Control work instructions
- Design a scalable digital workflow for biosimilar submissions
- Request GMP and registration documentation
- Track GMP and registration documentation
- Create a country-specific Quality database
- Cover testing requirements
- Cover transport validation requirements
- Cover notification requirements
- Cover QA obligations
- Perform stability data sanity checks
- Identify data gaps across markets
- Coordinate remediation efforts
- Ensure proper archival of data packages
Education
- Currently in higher education
Languages
- English – Business Fluent
Benefits
Mentorship & Coaching
- Mentorship from experienced leaders
Career Advancement
- Pathway to future roles
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Quality Biosimilars Advanced Studies Masters-level Internship(m/w/x)
Building a digital database for Innovation & Development at a global healthcare leader, ensuring Quality System compliance. Master’s student in Biotechnology, Pharmacy, Bioengineering, or related field required. Mentorship from experienced leaders, clear pathway to future roles.
Requirements
- Master’s student in Biotechnology, Pharmacy, Bioengineering, Quality Management, Life Sciences, or related field
- Strong analytical mindset and interest in Quality, regulatory pathways, and biosimilar development
- Ability to transform complex information into structured, digital solutions
- Self-driven, detail-oriented, and comfort with global collaboration
- Curiosity, initiative, and ambition for high-impact projects
Tasks
- Build a digital database for Innovation & Development
- Capture QA project data and lead assignments
- Support Quality System transition and maintenance
- Ensure Quality System compliance
- Ensure documentation readiness
- Define and implement standardized Change Control for biosimilars
- Develop Quality SharePoint for Change Control
- Create Change Control work instructions
- Design a scalable digital workflow for biosimilar submissions
- Request GMP and registration documentation
- Track GMP and registration documentation
- Create a country-specific Quality database
- Cover testing requirements
- Cover transport validation requirements
- Cover notification requirements
- Cover QA obligations
- Perform stability data sanity checks
- Identify data gaps across markets
- Coordinate remediation efforts
- Ensure proper archival of data packages
Education
- Currently in higher education
Languages
- English – Business Fluent
Benefits
Mentorship & Coaching
- Mentorship from experienced leaders
Career Advancement
- Pathway to future roles
About the Company
Abbott Products Operations AG
Industry
Healthcare
Description
Abbott is a global healthcare leader that helps people live more fully at all stages of life, with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.
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