Kenvue is currently recruiting for a:
Pharmacovigilance Analyst
What we do
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.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact 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:
GER SR FAMACOVIG LAN LPV
Location:
Latin America, Brazil, Sao Paulo, Sao Paulo
Work Location:
Fully Remote
What you will do
The Pharmacovigilance Analyst will support the Local Pharmacovigilance Organization in several LPV operations and compliance tasks related to the vigilance of the Kenvue product portfolio under the umbrella of the Local Safety Officers (LSOs). The Pharmacovigilance Analyst will work in close partnership with the LPVEx group, Regional Heads and Local Safety Teams to centralize activities to ensure consistent operations approach across the regions in alignment with the LPV processes for areas of responsibility, enabling process optimization and increasing efficiency.
You will collaborate with cross-functional teams to ensure patient safety and product efficacy:
Key Responsibilities
Support the LSOs on applicable operational tasks and coordinate communications to the LPV Organization. Work in close partnership with members of LPV across all regions to ensure a global consistent approach for Safety.
Manage the Group Mailbox and LPV SharePoint site
Oversee timely delivery of the requested Pharmacovigilance System Master File (PSMF) annexes per PV regions.
Key contributor for the Annex A (Contact details for Local PV Contacts Nominated at National Level) & C (Company Units responsible for safety data collection of solicited and spontaneous cases).
Ensure appropriate Quality checks being performed in accordance with PSMF Policies
Maintenance/generation of AE/PQC contact list for PVA contracts, LSO contact list and Art 57 lists to ensure accurate information is shared with others. Manage LPV members information (new hires, termination, etc.) on global data base.
Manage assignment of trainings per role, access to SharePoint and support addition on Distribution List, in close cooperation with Regional LPV Teams.
Support Local Pharmacovigilance Organization on the translation of regulatory requirement to reporting rules on the safety system.
Support on Investigations and CAPAs for LPV.
What we are looking for
Required Qualifications
Computer literate with knowledge of safety database systems, including reporting rules management and report generation.
Fluent communication skills in English, any additional language is a plus
Qualification in Medical/ Health Sciences and/or proven equivalent experience in pharmacovigilance and/or data management.
Excellent social, organizational, oral, and written communication & presentation skills.
Detail-oriented & compliance mindset skills.
Efficient, flexible, and dynamic team player.
Able to work effectively with different cultures and instill a culture of diversity and inclusion
Desired Qualifications
Experience with AI-driven pharmacovigilance platforms
Demonstrated ability to innovate within R&D environments using cutting-edge analytical methods
Exceptional skills in interdisciplinary collaboration bridging scientific research with computational tools
Passion for pioneering new solution for operational activities
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.