Quality Intern

🌟 사노피 코리아 인턴십으로 제약 커리어를 시작하세요! 

과학과 헬스케어 혁신에 관심 있다면, 글로벌 제약 리더 사노피(Sanofi) 와 함께 첫걸음을 내딛어보세요. 인턴십프로그램을 통해, 전공·경험과 상관없이 배우고 성장하고 싶은 분들을 환영합니다. 

왜 사노피 인턴십인가요? 

✨ 실무 프로젝트 참여 – 한국·글로벌 환자 치료에 영향을 주는 업무 경험 
🎓 전담 멘토링 – 제약사 업무 전문가와 1:1 성장 지원 
🚀 커리어 역량 강화 – 실무 학습·코칭·네트워킹 제공 
🌍 글로벌 환경 – 글로벌 제약회사의 선진 업무 환경 
💡 의미 있는 일 – 환자 삶을 개선하는 미션 중심 업무 

사노피에서는 여러분이 단순한 인턴이 아니라, 혁신을 함께 만드는 팀의 중요한 구성원입니다. 제약 산업에 대한 통찰을 얻고, 실무 역량을 키우며, 미래 커리어의 기반을 다질 수 있습니다. 

📩 지금 지원하고 헬스케어 혁신을 향한 여정을 시작하세요! 

Intern Position Title: Quality Intern

●       지원 대상: 대학교/대학원 재학생 (학사: 7학기 이상 수료 |석사: 3학기 이상 수료) 및 졸업유예/예정자

●       인턴십 기간: 2027년 1월 11일~ 2027년 7월 9일

●       소속 부서/팀: Quality/NPI & Quality System

●       업무 지역: 서울시 서초구 반포동 본사 사무실

About the job

Quality Intern - Seoul, Korea

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

Sanofi는 R&D 중심의 AI 기반 바이오파마 기업으로, 사람들의 삶을 개선하고 지속적인 성장을 이끌기 위해 노력하고 있습니다. 우리는 면역 체계에 대한 깊은 이해와 혁신적인 파이프라인을 바탕으로, 전 세계 수백만 명을 치료하고 보호하는 의약품과 백신을 개발하고 있습니다.

Sanofi는 과학의 기적을 추구하며, 함께 더 나은 삶을 만들어갑니다.

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

●      Support Audit & Inspection Readiness Checkto ensure that the organization maintains a state of compliance and control

●      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

●     Eligibility: Current university and graduate students (Bachelor's: completed 7 or more semesters | Master's: completed 3 or more semesters) and students with deferred or expected graduation

●       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

Required Application Documents (필수 제출서류) 

• Free-format Personal Statement (자유양식 자기소개서) and Resume (CV) in English

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

Pursueprogress, discoverextraordinary

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 ourALL IN video and check out our Diversity Equity and Inclusion actions atsanofi.com!