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IFF
Analyst, Regulatory Affairs
Posted on Nov. 18, 2024
- 11, South Korea
- 0 - 0 USD (yearly)
- Full Time
- Responsible for the preparation of regulatory submissions including dossiers for novel foods, processing aids, health claims and other relevant regulatory documents or submissions.
- Collaborate with internal IFF Global Regulatory Strategy Lead and relevant Global Product Managers to implement relevant strategic efforts for dietary ingredients in Korea, including probiotics, postbiotics, botanicals and bioscience ingredients.
- Responsible for providing regulatory guidance to IFF Quality team for aspects of product compliance including GMPs and product labeling.
- Assists in responding to customer inquiries.
- Provide regulatory assistance to logistics for shipment clearances.
- Maintain current knowledge of the developments and changes to regulations, industry standards, and assist in the dissemination of this information to the appropriate internal stakeholders
- Interpret new and existing regulatory requirements, policies, and guidance as they relate to the products and initiates actions to assure compliance to these regulations.
- Review of scientific literature and data from clinical trials to support health benefit statements and marketing of dietary ingredients and relevant products.
- Represent IFF at relevant industry groups and regulatory authorities including MFDS and regional associations.
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