Area Safety Lead (PV 약물 감시 - 계약직 채용)

Area Safety Lead (PV 약물 감시 - 계약직 채용)

O que fazemos

At Kenvue, percebemos o extraordinário poder do cuidado diário. Construída com base em mais de um século de herança e enraizada na ciência, somos a casa de marcas icônicas - incluindo NEUTROGENA®, AVEENO®, TYLENOL,® LISTERINE,® JOHNSON'S® e BAND-AID® que você já conhece e ama. A ciência é a nossa paixão; O cuidado é o nosso talento.

Quem somos

Nossa equipe global é de ~ 22.000 pessoas brilhantes com uma cultura no local de trabalho onde cada voz é importante e cada contribuição é apreciada. Somos apaixonados por insights, inovação e comprometidos em entregar os melhores produtos aos nossos clientes. Com experiência e empatia, ser um Kenvuer significa ter o poder de impactar milhões de pessoas todos os dias. Colocamos as pessoas em primeiro lugar, nos importamos ferozmente, ganhamos confiança com a ciência e resolvemos com coragem - e temos oportunidades brilhantes esperando por você! Junte-se a nós para moldar nosso futuro - e o seu. Para obter mais informações, clique em aqui.

Role reporta para:

Area Safety Lead, South Korea, HK &TW

Localização:

Asia Pacific, South Korea, Seoul, Seoul

Local de trabalho:

Híbrido

O que você fará

*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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