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HaleonPosted 3 weeks ago

Regulatory Affairs (Senior) Associate

On-siteSeoul, Seoul, South Korea

Full TimeSenior LevelEnterprise

Job Summary

Manage the overall life-cycle of Haleon products to ensure compliance with internal and external requirements, focusing on Quasi-drug and OTC classifications. Obtain new product registrations from the MFDS and handle packaging and promotional material review and approval. Monitor the Korea regulation environment and support the Korea RA Director in delivering the team's targets. This role requires 5+ years of related company and functional experience, basic English communication skills, and preferred OTC or Quasi-drug registration experience.

Required Qualifications

  • Basic English communication skill
  • OTC, Quasi-drug registration experience
  • Dietary supplement (Health functional food) experience

Desired Qualifications

  • 5+ years of related company & functional experience
  • Packaging & promotional material review & approval
  • Korea regulation environment monitoring
  • Support Korea RA Director to deliver team's target
  • Overall life-cycle management of Haleon products to be compliant to both Korea and Haleon policy
  • Obtain new product registration from MFDS
  • Product classification focused on Quasi-drug, OTC

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