Description

• For timely approval of biotech crop import approvals in Korea, prepare submission dossiers and response to government agencies’ questions by working with RAS colleagues and Leader in Korea, Regional Regulatory Manager, Global Regulatory Project Managers, and Regulatory Science Team, and follow through on agreed course of action.
• Ensure high quality, accuracy and timeline of the documents required for biotech crop approval/registration in Korea.
• Maintain up-to-date knowledge of regulatory policies and data requirement, analyze potential questions or issues, and effectively communicate and work with Corteva internal stakeholders to ensure all necessary actions are taken to meet requirements, and to track progress against projected milestones.
• Develop and sustain legitimate relationship with Corteva external customers and stakeholders, including regulators, for efficient communication to advocate Corteva’s values. 
• Comply with regulations, Corteva policy and core values, including ethics and company required trainings.

Qualifications

• PhD or MS in agricultural sciences, biochemistry or related fields, preferably at least 2 years of research or regulatory experience with the private or public sectors.
• Fluent in English both written and spoken.
• Good technical writing skills both in Korean and English. 
• Strong written, oral and interpersonal communication and presentation skills.
• Professional experience of product registration, especially with agricultural biotech products, agrichemicals or food additives will be an advantage.
• Ability to work in a multitasking environment and meet projected timelines.
• Ability to work independently as well as a team-player under collaborative environment.
• Must be available to travel as required (approximately 10% overseas).