職位描述
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. 工作職責：1.負責部門的樣品調度，分配和測試。 2.根據cGMP，FDA和ICH指導原則，安全要求，實驗室標準操作程序以及公司的政策和程序，創建和修改部門的測試程序。 3.提供實驗室和儀器儀表的技術支持。 4.和QA協作，提高質量體系。 任職資格：化學或相關領域的M.S. ，至少5年或以上的制藥經驗，1-2年的管理經驗。 具有良好的解決問題和溝通能力。 職位概覽 為配合公司實驗室建設及開展檢測業務，杭州艾品公司特此招聘以下各個部門的各類層次人員 (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：成功應聘者將由杭州艾品公司直接聘用并提供薪酬及福利待遇。所有雇員與長三角綠色制藥協同創新中心或其協同成立單位（包括浙江工業大學）將無任何形式的勞務關系。聯系方式 Contact Info： 人事經理 hr@irvinepharma-china.com 請按照下列格式書寫email主題：申請部門_職位_最高學歷_姓名。舉例，一位叫張三的申請者，最高學歷是碩士（MS），申請分析部門(Analytical Chemistry) 的HPLC Supervisor職位，則主題格式為：Analytical Chemistry_HPLC Supervisor_MS_Zhang San。同時，請按照同樣規則將所附簡歷命名。即其簡歷命名為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.
