Pharmacovigilance Specialist

Kenvue; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading health and wellness company is seeking a Pharmacovigilance Specialist in São Paulo, Brazil, who will support key pharmacovigilance processes and ensure compliance for the Kenvue product portfolio. With a requirement of a Bachelor's degree in a medical-related field and at least 3 years of experience, this role demands fluent English communication and an ability to connect globally. The position offers a competitive total rewards package and opportunities for development, in a fully remote environment.

Serviços

Competitive Total Rewards Package

Paid Vacation

Learning & Development Opportunities

Qualificações

• Qualification in Medical / Health Sciences and/or proven equivalent experience in pharmacovigilance.
• A minimum of 3 years’ experience.
• Good verbal and written communication skills.

Responsabilidades

• Support the LSOs on applicable tasks related to Vendor Service and Technical agreements.
• Work in close partnership with members of LPV across all regions.
• Creation and ownership of procedural documents and Job-aids for the VST Agreements Hub.

Conhecimentos

Fluent communication skills in English

Ability to connect in a global organization

Formação académica

Bachelor's degree in a medical-related field

Descrição da oferta de emprego

Kenvue is currently recruiting for a:

Pharmacovigilance Specialist

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.

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!

Role reports to

Mgr Loc Pharmacovigilance Contract Lead

Location

Latin America, Brazil, Sao Paulo, Sao Paulo

Work Location

Fully Remote

What you will do

This position reports directly to the Manager, LPV Contract Lead within the Local Pharmacovigilance (LPV) Organization and is based in São Paulo, Brazil.

As a Pharmacovigilance Specialist, you 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).

Key Responsibilities

• Support the LSOs on applicable tasks related to Vendor Service and Technical (VST) agreements and coordinate management efforts between the different applicable groups.
• Work in close partnership with members of LPV across all regions to ensure a globally consistent approach for Safety.
• Routine assessment of new safety‑related VST agreements from all regions for relevance to PSMF, presence of safety wording and other applicable requirements.
• Centralize contributions related to PSMF Annex B (Organizational Structure of the MAH) for VST Agreements from all regions.
• Work in partnership with applicable Training Management team to ensure new VST are covered regarding training and pharmacovigilance responsibilities awareness.
• Creation and ownership of procedural documents, WIs, SOPs, Job‑aids to reflect the work scope and responsibilities of the VST Agreements Hub to facilitate access and training of the applicable team.
• Management of training curricula for VST Agreements Hub members.

Required Qualifications

• Qualification in Medical / Health Sciences and/or proven equivalent experience in pharmacovigilance and safety issue management.
• Bachelor's degree in a medical‑related field (preferred).
• A minimum of 3 years’ experience.
• Fluent communication skills in English; any additional language is a plus.
• Ability to connect in a global organization.

Desired Qualifications

• 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
• Employee Resource Groups
• Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits.

Kenvue is proud to be an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment based on business needs.