Consultant

【求人No NJB2408584】
主に日本における農薬の規制承認分野において、当社の専門家をサポートしていただきます。
学際的なチーム内で円滑にコミュニケーションを図り、社内の他の業務・技術専門家や、社外のクライアント、規制当局と連携する能力が求められます。規制および技術的な観点から、さまざまな農薬関連製品の規制申請書類の作成を支援していただきます。
勤務地は日本の東京となりますが、業務範囲はアジア太平洋地域の他の国々にも及ぶ可能性があります。

【業務詳細】
・ 日本の農薬およびバイオラショナルに焦点を当て、プロダクト・スチュワードシップおよび安全性プロジェクトの実施を支援する
・ 学際的・国際的な規制関連プロジェクトにおいて、チームメンバーとして活動する
・ プロジェクトマネージャーの支援のもと、既存および今後の規制上の義務（環境、健康・安全関連の分野）についてクライアントに助言を行う
・ クライアントの申請書類や文献レビュー報告書の作成・提出、関係当局とのやり取り、試験の企画・実施およびモニタリング（例：有効性、毒性、環境中での挙動、残留物）の支援
・ 日本のクライアントとランボル（Ramboll）の国際的な同僚との間の連絡窓口としての役割
・ ランボル・ヘルスサイエンス・スピアヘッド（Ramboll Health Science Spearhead）内の国際チームと緊密に連携
・ その他のプロジェクト関連業務において、プロジェクトマネージャーを支援する

You will join our Environment and Health Business Unit
As our new Senior Consultant Health Science you will be supporting our subject matter experts mainly in the area of agrochemical regulatory approvals in Japan. You will bring the ability to communicate across an interdisciplinary team engaging with other business and technical professionals and externally with clients and regulatory agencies. From a regulatory and technical perspective you will support the preparation of regulatory submissions for a variety of agrochemical related products. A strong customer service ethic and ability to multitask is vital for this role. You will present a positive “can do” attitude and be a self starter within a team of dedicated professionals. Reporting to the Principal Health Sciences your role is based in Tokyo Japan and your scope of work might also cover other Asia Pacific countries.

Your key tasks and responsibility will be:
・ Support the execution of Product Stewardship and Safety projects with a focus on Japanese Pesticides and Biorationals
・ Act as team member for interdisciplinary / international regulatory projects
・ Advise clients on existing as well as upcoming regulatory obligations （in the fields of environmental health safety related topics） with the support of the Project Manager
・ Support with the preparation and submission of client dossiers and literature review reports interaction with respective authorities study organization and monitoring of study trials （e.g. efficacy toxicity environmental fate residues）
・ Act as interface between the Japanese client and international Ramboll colleagues
・ Work closely with our international team within the Ramboll Health Science Spearhead
・ Support the Project Manager on other project related tasks

【Required】
・ Bachelor's degree or higher in agriculture pharmacy biology veterinary medicine chemistry or a related field
・ A minimum of 5 years’ industry or consulting experience with plant protection product registration regulatory affairs for pharmaceuticals chemicals or related products
・ Experience in regulatory science
・ Outstanding communication skills both oral and written
・ Ability to handle multiple tasks and work streams in a fast paced environment while maintaining outstanding attention to detail and quality of deliverables
・ Experience/comfort with working in a virtual team with stakeholders across geographies
・ Excellent proficiency in MS PowerPoint Excel Word and Outlook
・ You are fluent in Japanese and English
・ At least you have the ability to effectively communicate in English in internal meetings and through email correspondence
・ You are a confident communicator and listener and like interacting with people

【Better】
・ Experience in the agrochemical industry multinational companies and/or research institutions
・ Previous experience in working within an international and multicultural organization would be a plus
・ Knowledge in toxicology ecotoxicology efficacy testing or study monitoring would be a plus
・ Experience with fertilizer or household chemicals would be a plus
・ Good project management and client communication skills
・ Good time management and organisational capabilities
・ Ability to grasp the big picture