Quality Intern at Sanofi Aventis US LLC

Seoul, , South Korea -

Full Time

Start Date

Immediate

Expiry Date

18 Jul, 26

Salary

0.0

Posted On

19 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Complaint management, Product batch release, Quality documentation, Data monitoring, Quality control, Regulatory compliance, Strategic thinking, Microsoft 365, Data analysis, Trend monitoring, Communication, Growth mindset, Learning agility

Industry

Pharmaceutical Manufacturing

Description

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! Global Terms & Conditions and Data Privacy Statement Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live. All in for Diversity, Equity and Inclusion at Sanofi - YouTube

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.