職責描述：
- 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
任職要求：
- 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

是一家中美合資的生物制藥公司，坐落于天津中新生態(tài)城。公司正在籌建包括研發(fā)、中試、質控及GMP生產等功能的大型生產基地，并陸續(xù)從國內外招聘優(yōu)秀人才，組建一流的研發(fā)及生產團隊。公司正在籌建的是中國規(guī)模最大之一的生物藥物生產設施，其研發(fā)、生產及質量控制等設施均達到歐美設計建造標準。第一期工程將在三年內投產運行。杰科生物預計未來一期、二期共建設十條生產線，滿足十多個生物藥物的大規(guī)模GMP生產，達到1000-1500人的規(guī)模，產品包括單克隆抗體、抗體融合蛋白、細胞因子、重組蛋白或DNA疫苗等。