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Pharmacovigilance Specialist

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Veröffentlichungsdatum:
Enddatum:
ID:
2507038096W

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Kenvue rekrutiert derzeit für a:

Pharmacovigilance Specialist

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.

Rollenberichte an:

Mgr Loc Pharmacovigilance Contract Lead

Standort:

Latin America, Brazil, Sao Paulo, Sao Paulo

Arbeitsort:

Vollständig remote

Was Sie tun werden

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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