仕事概要
職種 | 営業、事務、企画、物流系/物流管理、貿易手続き、調達、バイヤー、店舗開発 |
---|---|
業種 | 医療/ その他医療 |
雇用形態 | 未分類 |
ポジションレベル | その他 |
募集人数 | 1名 |
希望入社時期 | - |
必須語学力 |
英語 (流暢に話せるレベル) 日本語 (流暢に話せるレベル) |
活かせる語学 | - |
勤務時間 | その他 |
福利厚生・休暇 | |
ビザ取得支援 | - |
外国人従業員 | - |
仕事詳細
Company Overview
Global Healthcare company with strong presents and pipeline.
over 1000 employees worldwide
Job Description
This position is responsible to support the process development and operation of global and Japan regional logistics of products and materials for autologous clinical and commercial supply.
Responsibilities will include, but are not limited to, to the following:
• Manage global and regional 3rd party logistics provider, freight forwarders, customs brokers and transportation carriers to ensure proper handling of all products and materials.
• Drive and manage projects to ensure the specifications and deadlines are fulfilling expectations from product lifecycle management perspectives.
• Ensure operational procedures are maintained in accordance with various regulatory bodies including customs, PMDA, MLH and applicable local tax authorities. Monitor and communicate emerging regulation changes.
• Work closely with internal scheduling team to manage and resolve service partner escalations and shipment exceptions issues to keep shipment moving in a compliant and timely manner.
• Drive accountability of 3rd party logistics service provider performance (monthly, quarterly, annually) through comprehensive KPI’s analytics understanding that tracks, monitors, and identifies opportunities to improve CAR-T logistics process while optimizing expense.
• Manage logistics service provider relationship and contract adherence. Provide analytics for all phases of contract administration to ensure clear and unambiguous contract tasks are established and implemented.
• Develop, document, implement, manage and improve import export processes, procedures, SOPs, checklists and tools. Ensure all compliance standard and operating procedures are adhered to during import and export. Provide trainings to related internal and external business partners to increase awareness and compliance
• Support 3rd party and government led queries, audits, disclosures, submissions and reports
• Identify opportunities and support the creation of new business processes for improvements
• Lead cross-functional projects and convene cross-functional meetings to resolve issues
• Partner with other stakeholders to create and implement best practices
• Participate with the scale-up and commercialization of new products
• Develop and track appropriate KPI to drive results and continuous improvement
• Ensure strong collaborative relationship within Global Supply Chain group and externally with Commercial and Clinical to consistently elevate the quality of thinking and ideas applied to the business
Requirements
Skills/Knowledge Required:
• 5 to 8 years of overall relevant experience, including minimum of 3 years of experience in biopharma, diagnostics, or life science related companies is required. Previous experience in cell therapy or regenerative medicine is highly preferred
• Bachelor’s degree in International Business, Business Administration or Supply Chain management is preferred Expert knowledge of domestic / international transportation and 3rd party logistics management is preferred
• Experience in cold chain logistics of biologicals or regenerative medicine products and materials across the region
• Experience in Import Licensing, Export Licensing, Country of Origin, Valuation, Transfer Pricing, government agencies, including but not limited to PMDA and MLH.
• Experience with audits and disclosure practices
• A proven record of designing and implementing value added import and export policies and processes.
• Project management experience
• Strong interpersonal and communication skills
• Hands-on team leader and team player willing to work in an environment where individual initiative, accountability, and professional maturity are required
• Must have strong analytical skills
• Able to synthesize information into a presentation appropriate to the organizational-level of the audience. Able to summarize information concisely and communicate it using appropriate medium
• Must be able to work with limited day-to-day supervision.
• Strong PC experience, Microsoft Office Suite experience required including; Excel; Outlook; PowerPoint
• Native Japanese & English
Additional Job Information
Interested Applications please email to:
yandy.low@rgf-professional.com
面接について
連絡先
Sr. Logistics Manager
RGFタレントソリューションズ株式会社
1300 〜 1370 万円