职位描述
GC Supervisor is responsible for the scheduling, assigning and testing of samples for GC department. This position requires the ability to supervise employee and have good problem solving abilities. Must be knowledgeable in chromatography in general and all forms of gas chromatography, in particular. Create and revise departmental and test procedures, SOP’s etc. Comply with all cGMP regulations, FDA and ICH guidelines, safety requirements, laboratory SOPs and company policies and procedures. Issue reports and experimental results, etc. Support and train department technicians and associate chemists. Provide technical support in the maintenance of lab systems and instrumentation. Works with the management group to improve and implement the required quality systems. Works closely with QA staff to maintain and improve Quality Systems. Requires a M.S. in Chemistry or a related field and minimum 5+ year of pharmaceutical experience, 1 – 2 years of supervisory experience. Demonstrated ability to manage multiple projects and meet critical deadlines. Successful candidates must be proactive and creative, well organized, and have excellent communication skills. Create and revise departmental and test procedures, SOP’s etc. Comply with all cGMP regulations, FDA and ICH guidelines, safety requirements, laboratory SOPs and company policies and procedures. Issue reports and experimental results, etc. Responsible for assigning the training of new analysts, reviewing their training records. Responsible for reviewing all analytical data generated, sign and date notebook and initial job worksheet, before analyst inputs results into database. Responsible for ordering chemicals, standards, lab supplies, etc., in order to get the work done on time. Ensure that all instruments, used in their areas, are in good working conditions and that calibrations and maintenance records are up to date. Support and train all lab technicians and associate chemists. Provide technical support in the maintenance of lab systems and instrumentation. 工作职责：1.负责部门的样品调度，分配和测试。 2.根据cGMP，FDA和ICH指导原则，安全要求，实验室标准操作程序以及公司的政策和程序，创建和修改部门的测试程序。 3.提供实验室和仪器仪表的技术支持。 4.和QA协作，提高质量体系。 任职资格：化学或相关领域的M.S. ，至少5年或以上的制药经验，1-2年的管理经验。 具有良好的解决问题和沟通能力。 职位概览 为配合公司实验室建设及开展检测业务，杭州艾品公司特此招聘以下各个部门的各类层次人员 (Technician, Associate, Supervisor, and/or Managers): Analytical Chemistry; Analytical Development; Stability; Biopharma; Microbiology; Quality Assurance; Business Development & Marketing; Finance; Human Resources; MIS; ICVS; Corporate Planning & Scheduling; Purchasing & Facilities;注意：成功应聘者将由杭州艾品公司直接聘用并提供薪酬及福利待遇。所有雇员与长三角绿色制药协同创新中心或其协同成立单位（包括浙江工业大学）将无任何形式的劳务关系。联系方式 Contact Info： 人事经理 hr@irvinepharma-china.com 请按照下列格式书写email主题：申请部门_职位_最高学历_姓名。举例，一位叫张三的申请者，最高学历是硕士（MS），申请分析部门(Analytical Chemistry) 的HPLC Supervisor职位，则主题格式为：Analytical Chemistry_HPLC Supervisor_MS_Zhang San。同时，请按照同样规则将所附简历命名。即其简历命名为Analytical Chemistry_HPLC Supervisor_MS_Zhang San.If using email to forward resume, please follow the renaming rules below: Department_Position_Highest degree achieved_Last name First name. For example, an applicant named Zhang San wants to apply for the position of HPLC Supervisor in the department of Analytical Chemistry. The highest degree he had is M.S. Then please write email subject as Analytical Chemistry_HPLC Supervisor_MS_Zhang San. On the other hand, please rename the resume to Analytical Chemistry_HPLC Supervisor_MS_Zhang San as well.
