INTERNSHIP DETAILS

Quality Intern

CompanySanofi
LocationSeoul
Work ModeOn Site
PostedApril 20, 2026
Internship Information
Core Responsibilities
The intern will support complaint management processes and assist with product batch release activities, including documentation and reference standard management. They will also participate in product recall exercises and conduct monthly quality data monitoring to identify improvement opportunities.
Internship Type
full time
Company Size
157
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Headquartered in Paris, France, it is the fifth largest pharmaceutical company in the world [3] and is dedicated to the research, development, production and marketing of pharmaceutical products in seven main areas: cardiovascular disease, thrombosis, oncology, diabetes, central nervous system, internal medicine and vaccines.
About the Role

Intern Position Title: Quality Intern

  • 지원 대상 : 대학교  및 대학원 졸업예정자, 졸업유예자, 졸업자

  • 인턴십 기간: 2026년 7월 1일~ 2026년 12월 18일

  • 소속 부서/팀: Quality/Product Maintenance

  • 업무 지역: 서울 서초구 반포 본사 사무실

About the job

Join a quality network that ensures how Sanofi delivers in Korea — reliably, compliantly, and at scale.

In Quality, you will play a critical role in safeguarding product integrity and patient safety, while driving continuous improvement across local Quality operations. You will help ensure that life-changing treatments reach patients in Korea — consistently, efficiently, and in full compliance with local regulatory requirements.

 

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities (담당 업무):

  • Support complaint management processes by coordinating communication with investigation sites, complaint Hub, and local warehouse

  • Assist with product batch release activities, including reviewing packaging materials, vaccine documentation, and managing reference standards for local quality control

  • Participate in product recall exercises to ensure readiness for emergency response situations

  • Maintain quality documentation and records, ensuring proper archiving and organization of critical quality data

  • Conduct monthly quality data monitoring to identify improvement opportunities

  • Learn quality control operational procedures, including understanding reference standards and laboratory processes

About you

  • Preferred field of study: Pharmacy, Life-Science, Engineering

  • Fluency in written and spoken English is required in a global environment.

  • Demonstrates passion for the healthcare industry

  • Possesses strong strategic thinking skills

  • Digitally fluent

  • Shows learning agility and a growth mindset

  • Advanced proficiency in Microsoft 365

Why choose us?

  • Meaningful, real-world project experience contributing to patient care in Korea and beyond

  • Close mentorship with dedicated one-on-one guidance from experienced professionals

  • Structured development opportunities through hands-on learning, coaching, and networking

  • Exposure to a global healthcare environment, collaborating across functions and markets

  • Exposure to pharmaceutical quality systems (QMS) and how they operate in a regulated Good Distribution Practice (GDP) and Good Importing Practice (GIP) environment

  • Hands-on experience with quality documentation — Standard Operation Procedures (SOPs), deviations, Corrective Actions and Preventive Actions (CAPAs), and change controls

  • Opportunity to contribute to quality metrics reporting and Key Performance Index (KPI) tracking, gaining practical data analysis and trend monitoring experience

  • Exposure to real compliance challenges, with the opportunity to propose evidence-based, actionable solutions

  • Access to insights into the Korean pharmaceutical regulatory landscape (Ministry of Food and Drug Safety) and its alignment with global regulatory standards

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Key Skills
Complaint managementProduct batch releaseQuality documentationData monitoringQuality controlRegulatory complianceStrategic thinkingMicrosoft 365Data analysisTrend monitoringCommunicationGrowth mindsetLearning agility
Categories
HealthcareScience & ResearchEngineeringData & Analytics
Benefits
Meaningful project experienceClose mentorshipStructured development opportunitiesCoachingNetworking