Area Safety Officer

Was wir tun

Bei Kenvue erkennen wir die außergewöhnliche Kraft der täglichen Pflege. Aufbauend auf über einem Jahrhundert Tradition und verwurzelt in der Wissenschaft, sind wir das Haus der ikonischen Marken - darunter NEUTROGENA®, AVEENO®, TYLENOL,® LISTERINE®, JOHNSON'S® und BAND-AID®, die Sie bereits kennen und lieben. Wissenschaft ist unsere Leidenschaft; Fürsorge ist unser Talent.

Wer wir sind

Unser globales Team besteht aus ~ 22.000 brillanten Mitarbeitern mit einer Arbeitsplatzkultur, in der jede Stimme zählt und jeder Beitrag geschätzt wird. Wir sind leidenschaftlich an Erkenntnissen interessiert, Innovation und dem Engagement, unseren Kunden die besten Produkte zu liefern. Mit Fachwissen und Einfühlungsvermögen bedeutet ein Kenvuer zu sein, die Macht zu haben, jeden Tag Millionen von Menschen zu beeinflussen. Wir stellen den Menschen an die erste Stelle, kümmern uns leidenschaftlich, gewinnen Vertrauen in der Wissenschaft und lösen Lösungen mit Mut – und haben brillante Möglichkeiten, die auf Sie warten! Gestalten Sie mit uns unsere Zukunft – und Ihre. Für weitere Informationen, klicken Sie auf hier.

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Was Sie tun werden

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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