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 졸업자, 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 Check to 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(Degree in science or related field required)

• 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