Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
Area Safety Lead, South Korea, HK &TW位置：
Asia Pacific, South Korea, Seoul, Seoul工作地點：
混合你會做什麼
*This position is for replacement of maternity leave for one year. ( ~ Jul, 2026)
What you will do
Act as Local Nominated Person (including back-up nominated person)
- Function as nationally nominated person for Pharmacovigilance in respective countries assuming the PV role as defined by national law. Collaborate with the QPPV offices as required.
Oversight of the PV System & Overall responsibilities
- Provide oversight of vendor resources in the countries in scope.
- Record self-identified non-conformances and collaborating with the global team to investigate non-conformances while developing and implementing effective CAPAs.
- Support the Area Safety Head in providing relevant local information for the European Economic Area/UK Pharmacovigilance System Master Files while collaborating with the global team to meet requirements for local PSMFs if applicable
Safety Management & Reporting
- Maintain up-to-date knowledge of local requirements for pharmacovigilance, cosmetic and device vigilances including reporting requirements (for all applicable product classes in the territory) and collaborating with the global team to implement process changes required for identification of new requirements.
- Maintain oversight on day-to-day adverse Drug Reaction events inbound and outbound reporting as applicable in the given territory.
- Responds to safety-related health authority queries in the territory.
- Collaborating with the global and local teams to notify local health authorities of any safety issues including SSI/ESI and Signals.
- Collaborate with the local and global teams to ensure pharmacovigilance compliance of local company sponsored programs and research activities.
- Perform translation for ICSR and PV-related documents, as required.
Collaboration & Support
- Provide technical and strategic input and participate in projects/ workstreams led by the KMS teams or LOC.
Procedural Document Management
Audit & inspection readiness
PV contract management
Business Continuity Management
What we are looking for
- Health care science professional (preferably Physician or Pharmacist)
- +7 years of relevant experience
- Pharmaceutical industry experience including product vigilance responsibility role
- Ability to organize workflow activities and manage multiple critical issues
- Awareness of and familiarity with industry principles of product vigilance, drug development, and pharmacology
- Expert knowledge of global, regional, and local procedural documents as applicable
- Computer literate with knowledge of relevant IT safety systems
- Ability to establish and maintain open relationships within the organization and with authorities
- Demonstrable knowledge of all local requirements and of global aspects of product safety
- Fluency in the national language(s) and the English language.
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