Pharmacovigilance Specialist

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

Mgr Loc Pharmacovigilance Contract Lead

Lieu :

Latin America, Brazil, Sao Paulo, Sao Paulo

Lieu de travail :

Entièrement à distance

Ce que tu vas faire

Kenvue is currently recruiting for:

Pharmacovigilance Specialist, LPV Contract Hub

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

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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the 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.

What you will do 

The Pharmacovigilance Specialist 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 global 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, WI, 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.

What we are looking for

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

• Annual base salary. This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
• Competitive Total Rewards Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Employee Resource Groups 
• This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

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