Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Area Safety Head位置：
Asia Pacific, Indonesia, Jawa, Jakarta Raya工作地点：
混合你会做什么
Kenvue is currently recruiting for:
Area Safety Officer
Who we are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to: Area Safey Head
Location: Jakarta
Travel %:
What you will do
This role focuses on managing local pharmacovigilance and product safety activities, ensuring compliance with regulatory requirements. You’ll act as the main point of contact for safety reporting, handling adverse events, supporting health authority queries, and working closely with local and global teams to maintain proper processes, documentation, and overall safety compliance.
Key Responsibilities
Function as the nationally nominated person for Pharmacovigilance in respective countries, assuming Pharmacovigilance and/or Cosmetovigilance and/or Technovigilance roles, as defined by national law
Ensure 24/7 availability within the countries of responsibility, if required by national law
Collaborate with QPPV offices as required
Provide oversight of vendor resources in the countries in scope
Support the Area Safety Head in providing relevant local information for the European Economic Area/UK Pharmacovigilance System Master Files
Perform other agreed tasks assigned by the manager
Record self-identified non-conformances and collaborate with the global team to investigate and implement effective CAPAs
Safety Management & Reporting
Receive and support responses to safety-related health authority queries within the territory
Perform reconciliation with distributors, third parties, vendors, and internal stakeholders
Ensure proper identification of local literature articles for adverse event reporting
Manage document control, archiving, and compliance documentation
Ensure proper training and awareness of safety reporting responsibilities among local teams
Monitor regulatory changes and assess their impact on vigilance activities
Collaborate with global and local teams to notify health authorities of safety issues (including SSI/ESI and Signals)
Manage submission of safety reports and updates (e.g., SAE, SUE, SUSARs, PSUR, RMP) to local authorities and internal stakeholders
Maintain up-to-date knowledge of local pharmacovigilance, cosmetic, and device vigilance requirements
Ensure compliance of company-sponsored programs and research activities with pharmacovigilance requirements
Perform translation for ICSR and PV-related documents as required
Collaboration & Support
Support cross-functional collaboration across internal and external stakeholders
Perform translation for ICSR and PV-related documents as required
Procedural Document
Develop, update, and implement local procedures aligned with Kenvue global standards and national regulations
Maintain up-to-date knowledge of all relevant company procedures and training
Audit & Inspection Readiness
Ensure continuous readiness for audits and inspections
Maintain current knowledge of all relevant procedures and training
PV Contract Management
Support pharmacovigilance contract management activities
Maintain current knowledge of all relevant procedures and training
Business Continuity
Support business continuity planning related to pharmacovigilance activities
Maintain current knowledge of all relevant procedures and training
What We Are Looking For
Required Qualifications
Education: Healthcare or life sciences background (preferably Physician or Pharmacist)
Minimum 3 years of relevant experience
Desired Qualifications
Experience in the pharmaceutical industry, particularly in product vigilance roles
Strong knowledge of general medicine, pharmacy, clinical practice, or related scientific fields
Proven ability to organize and manage workflow effectively
Familiarity with pharmacovigilance principles, drug development, and pharmacology
Knowledge of global, regional, and local procedural documents
Proficiency in relevant IT safety systems and general computer skills
Strong verbal and written communication skills
Ability to build and maintain relationships with internal stakeholders and regulatory authorities
Demonstrated knowledge of local and global product safety requirements
Fluency in local language(s) and English
What we are looking for
Required Qualifications
- Education: Health care science professional e.g.: (preferably Physician or Pharmacist)
- At minimum 3 years’ experience.
Desired Qualifications
- Pharmaceutical industry experience including product vigilance responsibility role.
- Sound knowledge of general medicine, pharmacy, and clinical practice, or another relevant scientific/medical field.
- Proven ability to organize workflow activities.
- Awareness of and familiarity with industry principles of product vigilance, drug development, and pharmacology.
- Knowledge of global, regional, and local procedural documents as applicable.
- Computer literate with knowledge of relevant IT safety systems.
- Good verbal and written communication skills.
- 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.
What’s in it for you
· Competitive Benefit Package
· Learning & Development Opportunities
· An opportunity to partner with leadership teams in bringing in the best talent on board!
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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