A. Obtain timely and cost effective approvals for biotechnology plant products in Korea.
1. Develop the product approval plans, working with Supervisor, Regional Coordinator, Global Registration Team and Country Management, and follow through on agreed course of action.
2. Maintain current knowledge of bio-safety regulatory data requirements of relevant government agencies.
3. Compile regulatory data packages for product approval/registrations that conform to Korean biotech regulations.
4. Prepare for the responses to the questions from government agencies regarding safety assessment of the product
B. Provide technical and regulatory information to support product launch in biotech plant cultivation countries.
C. Promote a favorable environment for biotechnology plant products.
경력 및 자격요건
•Ph.D. in plant biotechnology or biology related majors, or MS with at least 5 years of relevant experience.
•Communication and negotiation skills.
•Capability to work in a multitasking environment and meet deadlines.
•Fluent in English both written and spoken.
•Presentation skills.
•Good interpersonal communication and negotiating skills.
•Must be available to travel as required (approximately 10% overseas).
•Experience in risk assessment or toxicology related area or allergology is an advantage..
•Experience in the Korean government agencies or government relations field is an advantage
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-5042
hjunb@nterway.com
