Quality Biosimilars Advanced Studies Masters-level Internship

JOB DESCRIPTION:

Advanced Studies Intern Quality (Biosimilars)

Abbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.

Our medicines business is committed to bringing the benefits of our trusted medicines to more people in the worlds fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology womens health cardiometabolic pain management/central nervous system and respiratory.

Quality Biosimilars Advanced Studies Masters-level Internship

The Opportunity

This position is based at our Basel location in our medicines business (EPD).

Are you a highly motivated Masters student with a passion for biotechnology market launches quality systems and long-term operational scalability Join our Biosimilars Quality organization and contribute to initiatives that directly impact global patient access. This internship offers the opportunity to work at the intersection of science digital innovation and quality excellencealongside experts who are driving the next generation of biosimilar development.

You will take ownership of highvisibility projects that strengthen our Quality framework across multiple biosimilar assets regions and functions. This role is ideal for top-tier students seeking meaningful responsibility exposure to senior leaders and a handson experience within a complex internationally networked environment.

What You Will Work On

• Build a digital database for Innovation & Development capturing QA-relevant project data and lead assignments.
• Support the transition and maintenance of the Quality System ensuring compliance and documentation readiness.
• Define and implement a standardized Change Control (CC) process for MBX and other biosimilars including a Quality SharePoint and work instructions.
• Design a scalable digital workflow for requesting and tracking GMP and registration documentation for biosimilar submissions.
• Create a country-specific Quality requirements database covering testing transport validation notifications and QA obligations.
• Perform stability data sanity checks identify gaps across markets coordinate remediations and ensure proper archival of data packages.

What You Bring

• Masters 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 comfortable collaborating globally.
• Curiosity initiative and ambition to contribute to high-impact projects.

What Youll Gain

• Hands-on experience advancing real biosimilar programs.
• Exposure to global Quality regulatory strategy and product development.
• Project ownership with visible organizational impact.
• Mentorship from experienced leaders in Quality and Biosimilars.
• A pathway to future roles in Quality Regulatory Affairs or Biologics CMC.

If this sounds like the right opportunity for you wed love to hear from you. Please submit your CV (PDF format preferred). We welcome applicants from all backgrounds and are committed to building a diverse and inclusive team.

The base pay for this position is

In specific locations the pay range may vary from the range posted.

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