职责描述：
- Perform clerical and physical tasks in connection with all facets of CGMP material handling activities per standard operating procedures (sops)
- Issue and maintain inventory of general operational and scientific supplies including handling of investigational drug products, hazardous chemistry and heavy (~25 kg.) items
- Perform receipt process, reconcile delivered goods with purchase orders and resolve discrepancies in coordination with procurement staff
- Use electronic systems to record inventory related activities
- Operate material handling equipment such as pallet jacks, carts, and reach truck/forklift
- Perform daily administrative tasks such as inventory cycle counts and chart changing for chart recorders
- Arrange and coordinate storage and distribution of warehoused goods
- Provide shipping support, process, package and ship orders accurately
- Inspect materials for defects and damages
- Check, verify and fill laboratory requests
- Abide by all company safety and hygiene regulations
- Maintain cGMP cold storage freezer inventory
任职要求：
- Possession of high school diploma or equivalent.
- Minimum of two (2) years related experience
- General knowledge of inventory practices and procedures in a regulated environment
- Knowledge of inventory practices and experience with electronic inventory systems
- Ability to obtain hazardous materials certification within 1 year
- Knowledge of hazardous and International shipping
- Ability to operate material handling equipment (pallet jack, reach truck)
- Ability to effectively maintain accurate logs and records
- Basic computer skills for data entry and retrieval
- Ability to carry out physical tasks associated with this position:
- Lift and carry up to 50 lbs.; work involves walking, standing, kneeling, bending and stooping, potential exposure to particulates, compressed gases, refrigerated/frozen spaces, noisy environment and being around moving objects and/or vehicles

是一家中美合资的生物制药公司，坐落于天津中新生态城。公司正在筹建包括研发、中试、质控及GMP生产等功能的大型生产基地，并陆续从国内外招聘优秀人才，组建一流的研发及生产团队。公司正在筹建的是中国规模最大之一的生物药物生产设施，其研发、生产及质量控制等设施均达到欧美设计建造标准。第一期工程将在三年内投产运行。杰科生物预计未来一期、二期共建设十条生产线，满足十多个生物药物的大规模GMP生产，达到1000-1500人的规模，产品包括单克隆抗体、抗体融合蛋白、细胞因子、重组蛋白或DNA疫苗等。