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Sr. Regulatory Affairs Special |
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- Maintain and strengthen communication with Korean Food and Drug Administration (KFDA)
- Review, analyse and co-ordinate data for new product submissions
- Develop registration strategies, implement regulatory plan and co-ordinate multiple
projects and activities in accordance with strategic company objectives.
- Ensures timely preparation of valid submissions organized and scientifically
- Liaise and negotiate with the relevant authorities to facilitate and secure expeditious
regulatory approvals.
- Maintain the registration of marketed products.
- Provide regulatory input and support for marketing plans, product launches and other
cross-functional activities.
- Monitor and disseminate information on changes to regulations affecting registration,
manufacture, distribution and sale of products |
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- At least 7years experience in a regulatory position in industry
- Good Command of English |
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Nego. |
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~ 12. 2. 15 ±îÁö |
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02-597-1780 |
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[Á¢¼ö¹æ¹ý] E-mail : jiko01@kohuman.com (À̸ÞÀÏ Á¢¼ö¸¸ °¡´É) |
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