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J&J Family of Companies Japan Country Safety Officer (Fixed-Term Employee) in Tokyo, Japan

Japan Country Safety Officer (Fixed-Term Employee) - 2407018449W

Description

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 Dr.Ci:Labo®, NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact 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.

What You Will Do

Japan Country Safety Officer is responsible for the coordination and execution of post-marketing safety management activities for JNTL Consumer health K.K.

  • to ensure that all of local regulatory requirements, Kenvue and ethical responsibilities are met.

  • Local official company name in Japan.

Key Responsibilities

ž Ensure mechanisms in place to collect and receive adverse events from the various source, in partnership with the customer call center and other functions involved.

ž Ensure that local processes and systems are in place for tracking, processing, submission and conducting follow up for Adverse Events (AE) and other safety information. The scope of the product is OTC-drug, Medical device, Cosmetics and Quasi-drug.

ž Manage external vendor for local case processing.

ž Have communication with global stakeholders to solve the problems.

ž Ensure local/global medical or scientific literatures are reviewed to identify possible adverse events.

ž Maintain oversight of all required PV regulatory reporting compliance in a timely manner.

ž Ensure all required documents related to PV departmental activities are retained according to regulatory requirements.

ž Ensure all local PV quality documents are reviewed and updated as applicable.

ž Escalate compliance issues in a timely manner to Line Manager to ensure appropriate mitigation is implemented.

ž Ensure PV inspection/audit readiness at the affiliate level at all times.

ž Maintain awareness of local PV legislation and guidelines.

ž Work collaboratively with other functions and regional affiliates to ensure implementation of new company policies and regulatory requirements.

Qualifications

What We Are Looking For

Required Qualifications

  • 23 years’ experience working in the pharmaceutical industry is strongly preferred; PV related experience is an advantage

  • Business level English: listening, writing, speaking

  • Ability to work independently but collaboratively in a matrix organization

  • Knowledge of PV regulations

  • Demonstrated attention to detail

  • Excellent written and spoken communication and presentation skills.

Desired Qualifications

  • Medical, pharmacy or life-sciences degree (or equivalent)

  • Experience using global safety database desirable

Primary Location Asia Pacific-Japan-Tokyo-To-Chiyoda

Job Function Administration

Req ID: 2407018449W

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