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.

QUALIFICATIONS:

Describe the minimum knowledge, skill, related experience, and ability requirements for the position.

EDUCATION:

Health care science professional (preferably Physician or Pharmacist)

YEARS OF RELATED EXPERIENCE:

4-6 years of relevant experience.

KNOWLEDGE, SKILLS, ABILITIES:

Include any required computer skills, certifications, licenses, languages, etc.

• Pharmaceutical industry experience including product vigilance responsibility role.
• Ability to organize workflow activities and manage multiple critical issues.
• Experience with vendor resource oversight.
• Awareness of and familiarity with industry principles of product vigilance, drug development, and pharmacology.
• Expert knowledge of global, regional, and local procedural documents as applicable.
• Computer literate with knowledge of relevant IT safety systems.
• Excellent verbal and written communication skills.
• Ability to establish and maintain open relationships within the organization and with authorities.
• Demonstrable knowledge of all local requirements and of global aspects of product safety.
• Fluency in the national language(s) and the English language.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation

OVERSIGHT OF THE PV SYSTEM & OVERALL RESPONSIBILITIES

• Provide oversight of vendor resources in the countries in scope.
• Managing and coaching of the direct reports if applicable.
• Act as a delegate for the Area Safety Head, when required.
• Record self-identified non-conformances and collaborating with the global team to investigate non-conformances while developing and implementing effective CAPAs.
• Support the Area Safety Head in providing relevant local information for the European Economic Area/UK Pharmacovigilance System Master Files while collaborating with the global team to meet requirements for local PSMFs if applicable.