SHISEIDO KOREA
에이비일팔공(AB180)

[노보노디스크] Quality Assurance Manager 경력직 모집

서울 송파구 바이오,의약,제약 2026.04.30 ~ 채용시

Tasks

현재 노보노디스크제약에서 QA Manager로서 근무해주실 분을 찾고 있습니다.
관련 경력자 분들의 많은 지원 바랍니다. 


[직무 내용]
Novo Nordisk Pharma Korea (NNPK)의 전반적인 Quality Compliance process 담당
Quality Management System (QMS)의 관리 및 개선 (본사 및 국내 QA/QC 관련 규제사항 반영) 
내부 quality 관련 audit process 담당
외부 Quality Control 진행 관련 모니터링 

Location
 
This job location is Novo Nordisk Office in Jamsil, Songpagu-district.
 
Lead quality excellence in one of APAC's fastest-growing markets, where your expertise will directly impact patients across Korea while shaping the future of pharmaceutical quality standards.
 
Your new role
 
As Quality Assurance Manager, you'll be the cornerstone of quality excellence for Novo Nordisk South Korea, ensuring our life-changing medicines reach patients with unwavering quality standards. This is a pivotal leadership role where you'll implement and maintain our Quality Management System while serving as the legal Qualified Responsible Person for medicinal products.
Your responsibilities will include:
• Leading the implementation and maintenance of Novo Nordisk's Quality Management System (QMS) across the affiliate, ensuring full compliance with internal standards and external regulatory requirements
• Acting as Quality Management Representative for South Korea, serving as the primary point of contact with local Health Authorities during audits and inspections
• Managing critical quality processes including deviation handling, potential recalls, product release, returns, and destruction for all Novo Nordisk-owned products
• Conducting and coordinating quality audits as Lead Auditor for both internal operations and external partners, including distribution partners and clinical trial depots
• Serving as legal Responsible Person with registered pharmacist duties, including Import Manager and Wholesaler Business Manager roles in accordance with Korean regulations
• Leading and developing a team of 4 quality professionals while managing the QA team budget; Partnering with cross-functional teams to drive quality process improvements and simplification initiatives aligned with global expectations
 
Your new department
Novo Nordisk South Korea is a dynamic affiliate in a high growth phase, with a strong purpose to bring life-changing products to people living with Diabetes, Obesity and other serious chronic diseases. Recently certified in APAC as a Great Place to Work, we pride ourselves on continually striving for the best performance to meet our purpose, and to live the Novo Nordisk Way, which includes an absolute commitment to Business Ethics, Compliance and Quality. You'll report to the Legal, Compliance and Quality (LCQ) Director and play a vital role in maintaining our license to operate while supporting our ambitious growth trajectory. This is a people managing role with 4 team members.
 
Your skills & qualifications
We're looking for an experienced quality professional who thrives in a fast-paced, regulated environment and is passionate about ensuring patient safety through excellence in quality management. You'll bring with you:
• 10–18 years of progressive experience in Quality within the pharmaceutical industry or with a regulatory authority. Experience in a  global MNC or matrix organization is an advantage
• A valid Korean Pharmacist license is required to serve as the Responsible Person
• 2–3 years of people management experience, with a proven ability to lead, develop, and coach quality teams
• Strong expertise in QA processes, SOPs, compliance, GDP, and pharmaceutical distribution requirements, with working knowledge of QC analytical methods in chemistry and biological testing; In-depth knowledge of local and international regulations, with hands-on experience in pharmaceutical operations, quality control, and distribution
• Strong interpersonal, communication, stakeholder management, and people leadership skills, with a collaborative, resilient, and agile approach
• Native-level fluency in Korean language with strong English communication skills to work effectively in a global environment
 
Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.
 
Contact
Kindly upload your CV to our online career page (click on Apply and follow the instructions).
Internal candidates are requested to inform their line manager when applying. 
 
Deadline
Until the completion of recruitment. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.  

Requirements

  • QA processes, SOPs, and Compliance guidelines 관련 직무 지식 필수 
    제약산업에서의 유관 경력 약 10년 이상 (10-18년 경력자 선호)
    글로벌 조직에서의 근무경험 우대 
    대내외 stakeholder 협업 및 영어 능통자 모집
    약 2-3년의 Team management 경험이 있으신 분 선호
    분석적인 사고를 갖추신 분
    기본적인 컴퓨터스킬 (Microsoft Excel 포함) 갖추신 분
  • 10-18 years of progressive experience within the quality function of the pharmaceutical industry or with regulatory agencies. Pharmacist certification is mandatory.
  • Minimum 2-3 years of people management experience
  • Knowledge and experience in pharmaceutical operations, quality control, distribution and international regulations are essential and Global MNC / Matrix Organization experience is a plus
  • Good knowledge of QA processes, SOPs, and Compliance guidelines, including proficiency in GDPs and the requirements for pharmaceutical products distribution
  • Strong interpersonal and communication skills with supportive, persuasive, passionate and energetic mindset
  • Korean language fluency as well as English communication skills are required.

Information

커리어 수준
경력여부
경력
고용형태
정규직
급여사항
면접 후 협의

Apply

전형방법

1차 서류전형
2차 면접 전형 (부서 면접)
3차 면접 전형 (프리젠테이션 면접)

제출서류

자유양식의 CV 접수

접수방법
채용담당
블라인드 되었습니다.

The Others

면접은 서류전형 합격자에 개별통지 합니다.
국가보훈대상자와 신체장애자는 관련서류 제출시 관계법에 따라 우대함.
모든 서류는 반드시 MS Word로 작성하기 바랍니다.
제출하신 서류는 일체 반환하지 않습니다.
입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.
기타 문의사항은 E-mail로 문의바랍니다.

Company

외국계기업 제약바이오
서울 송파구 신천동 7-11 한국 광고 문화 회관 16층

full.png?from=upload


노보노디스크제약(주)는 덴마크 코펜하겐을 본사로 둔 글로벌 제약사로, 당뇨 인슐린 분야 글로벌 Market leader로 자리하고 있으며 2025년 기준 한국 지사 약 280명, 매출액 약 6953억원 규모의 회사입니다. 현재 당뇨 분야 외에 비만치료, 혈우병, 성장호르몬 영역의 비즈니스를 운영 중에 있으며 이 외 각종 만성질환 등 다양한 치료 영역의 제품이 임상 중에 있습니다. (사무실 위치: 송파구 잠실)


지속적인 혁신과 개발을 바탕으로, 빠르게 성장하고 있는 글로벌 제약사에서 함께 일할 능력있는 인재를 찾고 있습니다.

직무 품질보증 매니저
🛠 관련 기술 QMS QA SOP GDP Microsoft Excel
핵심 업무
  • 전사 품질 컴플라이언스 프로세스 관리
  • 품질경영시스템(QMS) 운영 및 개선
  • 내부 품질 감사 프로세스 담당
  • 외부 품질관리 진행 모니터링
  • 품질 이슈 처리, 리콜, 제품 출하, 반품, 폐기 관리
  • 내부·외부 감사 및 규제기관 대응
  • 품질팀 리딩 및 팀원 육성
  • QA 팀 예산 관리 및 협업 기반 개선 과제 추진
필수 요건
  • 제약산업 또는 규제기관 품질 분야 10년 이상 경력
  • 한국 약사 면허 보유
  • 2~3년 이상 팀 관리 경험
  • QA 프로세스, SOP, 컴플라이언스 가이드라인 및 GDP 지식
  • 제약 운영, 품질관리, 유통 및 국제 규정 관련 경험
  • 한국어 원어민 수준 및 영어 커뮤니케이션 능력
우대 요건
  • 글로벌 조직 또는 MNC/매트릭스 조직 근무 경험
  • 분석적 사고 역량
  • 기본 컴퓨터 활용 능력
BETAAI가 공고 원문에서 추출한 참고 정보입니다.
Chat with GPT

본 정보는 개인 구직자들의 취업지원을 위해 외국기업취업전문사이트 피플앤잡에서 수집한 정보이며, 채용회사의 사정에 따라 변경될 수 있습니다.
본 정보는 피플앤잡의 동의 및 허락 없이는 재배포 할 수 없습니다.