
高效液相色譜實(shí)驗(yàn)室主管 HPLC Supervisor

職位描述
HPLC Supervisor is responsible for the scheduling, assigning and testing of samples for HPLC department. This position requires the ability to supervise employee and have good problem solving abilities. Create and revise departmental and test procedures, SOP’s etc. Must be knowledgeable in chromatography in general and all forms of liquid chromatography, in particular. 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 to 10+ year of pharmaceutical experience, 2 – 3 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. 60%: Perform Lab Testing20%: Support Documentation Efforts20%: Support and Train工作職責(zé):1.負(fù)責(zé)該部門(mén)安排、分配和測(cè)試樣品。2.建立、修改部門(mén)的和測(cè)試程序、 SOP等。 3.為實(shí)驗(yàn)室系統(tǒng)和儀器維修提供技術(shù)支持。 4.協(xié)助QA,保證和提高質(zhì)量體系。 任職資格:M.S, 化學(xué)或相關(guān)領(lǐng)域。 具備5-10年或以上的制藥經(jīng)驗(yàn);2 - 3年的管理經(jīng)驗(yàn)。有良好的解決問(wèn)題的能力和良好的溝通技巧。 60%:執(zhí)行實(shí)驗(yàn)室測(cè)試 20%:支持文檔編寫(xiě)20%:支持和培訓(xùn)職位概覽 為配合公司實(shí)驗(yàn)室建設(shè)及開(kāi)展檢測(cè)業(yè)務(wù),杭州艾品公司特此招聘以下各個(gè)部門(mén)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(yīng)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(zhǎng)三角綠色制藥協(xié)同創(chuàng)新中心或其協(xié)同成立單位(包括浙江工業(yè)大學(xué))將無(wú)任何形式的勞務(wù)關(guān)系。聯(lián)系方式 Contact Info: 人事經(jīng)理 hr@irvinepharma-china.com 請(qǐng)按照下列格式書(shū)寫(xiě)email主題:申請(qǐng)部門(mén)_職位_最高學(xué)歷_姓名。舉例,一位叫張三的申請(qǐng)者,最高學(xué)歷是碩士(MS),申請(qǐng)分析部門(mén)(Analytical Chemistry) 的HPLC Supervisor職位,則主題格式為:Analytical Chemistry_HPLC Supervisor_MS_Zhang San。同時(shí),請(qǐng)按照同樣規(guī)則將所附簡(jiǎn)歷命名。即其簡(jiǎn)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.
企業(yè)簡(jiǎn)介
杭州艾品醫(yī)藥科技有限公司由浙江工業(yè)大學(xué)獨(dú)資創(chuàng)立,憑借與美國(guó)IPS公司的全面合作及長(zhǎng)三角綠色制藥協(xié)同創(chuàng)新中心提供的全方位支持,專注于為意在出口制劑、原料藥等產(chǎn)品到歐美市場(chǎng)的在華醫(yī)藥生產(chǎn)企業(yè)提供符合美國(guó)FDA認(rèn)可的全面藥品質(zhì)量檢測(cè)及其它相關(guān)服務(wù)。 長(zhǎng)三角綠色制藥協(xié)同創(chuàng)新中心是教育部、財(cái)政部批準(zhǔn)的首批14個(gè)“2011協(xié)同創(chuàng)新中心”之一,由浙江工業(yè)大學(xué)牽頭,聯(lián)合浙江大學(xué)、上海醫(yī)藥工業(yè)研究院、藥物制劑國(guó)家工程研究中心、浙江省醫(yī)學(xué)科學(xué)院、浙江省食品藥品檢驗(yàn)研究院等作為核心共建單位,由共同致力于提升科技創(chuàng)新能力和拔尖創(chuàng)新人才培養(yǎng)能力、服務(wù)和引領(lǐng)制藥產(chǎn)業(yè)轉(zhuǎn)型升級(jí)的高等院校、科研院所、企業(yè)和國(guó)際創(chuàng)新機(jī)構(gòu)等單位聯(lián)合組成。
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熱門(mén)區(qū)域招聘: 重慶 北京 上海 浙江 江蘇 廣東 山東 湖南 安徽 河北
浙江招聘企業(yè): 浙江佐力藥業(yè)股份有限公司 河南宛東藥業(yè)有限公司 杭州安杰思醫(yī)學(xué)科技有限公司 浙江中法制藥有限公司 貴州益佰制藥股份有限公司 福成堂大藥房 杭州杏園科技有限公司 杭州諾康醫(yī)療器械有限公司 浙江正京元大藥房連鎖有限公司 杭州明興生物科技有限公司
職位發(fā)布日期: 2015-01-16

