Kenvue is currently recruiting for a: Pharmacovigilance Analyst [12 months fixed term] What we do AtKenvue, 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, clickhere .Role reports to: Mgr Loc Pharmacovigilance Contract Lead Location: Latin America, Brazil, Sao Paulo, Sao Paulo Work Location: Fully Remote What you will do The Pharmacovigilance Scientist Analyst will support the Local Pharmacovigilance Organization in several PV processes and compliance tasks related to the vigilance of the Kenvue product portfolio, under the umbrella of the Local Safety Officers (LSOs).There as Lead Candidate identified, but all candidates are welcomed to applying.Responsibilities Support the LSOs on applicable operational tasks and ensure overall inspection readiness across the Local Pharmacovigilance Organization, collaborating closely with team members from all regions to ensure a consistent global approach to Safety.PV Contract Management Manage and maintain oversight local PV agreements across all regions. Ensure local agreements are reviewed to assess if a Pharmacovigilance (PV) agreement is recommended. Review the draft PV Agreement to ensure its accuracy and support negotiation with External Partners and execution in partnership with LSOs. Ensure accuracy of PSMF Annex B Service and Technical Agreements listing. Contribute to process improvement initiatives related to local PV agreement management. Procedural Document: Develop, update, and implement LPV procedures to ensure compliance with Kenvue global procedures and local requirements. Ensure current knowledge of all relevant company procedures and training.What we are looking for Desired Qualifications Qualification in Medical/ Health Sciences and/or proven equivalent experience in pharmacovigilance and safety issue management Experience in the Pharmacovigilance space Fluent communication skills in English. Ability to connect in a global organization.Desired Qualifications fluency in an additional language is a plus. 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.What's in it for you Competitive Total Rewards Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvue Impact NetworkGroups This list could vary based on location/regionIf you are an individual with a disability, please check ourDisability Assistance pagefor information on how to request an accommodation.