• 招聘类型：社招
• 工作性质：全职

职位描述

1.Create, according to the consolidated clinical demands, supply plans and develop production schedules for clinical trial materials to align with study timeline.

2.Manage production schedules to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans by working with supply chain lead and CMC project manager

3.Monitor the inventory to ensure accurate and continuous supply.

4.Cooperate with QA and logistics team to support other operation activities like labelling, shipment and ID test et al.

5.Lead cross functional projects and process improvements related to drug supply planning. 

任职条件

Education: Bachelor or Master Degree in Science or Business Administration, Operations Management, or similar education required, Supply Chain Management, and/or Management of Science or equivalent filed is preferred.

Experience: 4-5 years progressive experience in Supply Chain preferably within the biotech, pharmaceutical, CRO, and industry.

Work Skill:

1.Understands comprehensive global pharmaceutical regulatory requirements (e.g. cGMP, GDP, and/or GCP).

2.Broad operations and systems experience, including replenishment planning, capacity analysis, manufacturing and distribution in either a clinical or commercial environment

3.Experience in vendor oversight and managing external partnerships and relations.

4.Excellent interpersonal and communication skills

5.Excellent team player

6.Strong analytical and problem-solving skills

7.Demonstration of leadership and coaching skill

职位要求

• 学历要求：本科及以上
• 工作经验：4年以上
• 外语要求：English

公司福利

• 五险一金 
• 晋升空间 
• 法定节假日