美國藥典誠聘實驗室分析員(方法開發(fā)驗證)
日期:2013-06-27?
來源:丁香園
除美國之外,USP標(biāo)準(zhǔn)和標(biāo)準(zhǔn)品在的世界上其他130多個國家也得到廣泛的使用。建立185年以來,這些標(biāo)準(zhǔn)一直服務(wù)于世界各地,確保公眾獲得優(yōu)質(zhì)的藥品。
Position Title Scientist III / IV, Excipient
Job Type: ?Full-Time?
Reports To: Director, Medicine Compendium
Location: ?Zhangjiang Hi-Tech Park, Pudong, Shanghai?
Post Date: ?25/06/2013?
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Function of the Position:
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As a member of the Analytical Sciences group, the successful candidate will play a leading role on new and ongoing analytical proceduredevelopment for USP Medicine Compendiumprograms.
Interpret observations/results, and present data in scientific meeting /management meeting internally/externally.
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Roles and Responsibilities:
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· ? ? ? ? ? Lead analytical proceduredevelopment for characterizationandtesting of drug substances,excipients anddrug product. Conductanalytical procedurevalidation according to pre-approvedprotocol.
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· ? ? ? ? ? Provide technical expertise in planning, monitoring, and maintaining project timelines to meet business needs.
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· ? ? ? ? ? Present the results of your work internally and externally, and write reports that will be submitted to USP expert committee. Conduct all activities in compliance with established regulatory requirements. Assist in the development of protocols to conduct studies in conjunction with others to meet requirements.
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· ? ? ? ? ? Understand and complywith Safety, Good Laboratory Practice/Good ManufacturePractices (GLP/GMP), and Standard Operating Procedures(SOP)and Policies.
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· ? ? ? ? ? Record, evaluate, interpret and summarize technical data. Develop and validate calculation procedures. Document activities in technical notebooks or validated approved electronic media. Design experiments and preparereports, memosor documents with little direct guidance.
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· ? ? ? ? ? Maximize innovation by utilizing original concepts and creative thinking.
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· ? ? ? ? ? Can shift priorities and projects as organizationneeds change. As needed, assist others as priorities change. Observe safety rules and works safely in the laboratory.
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· ? ? ? ? ? Plan and track analytical development objectives, timelines, priorities, and resources
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· ? ? ? ? ? Mentorship and management of internal analytical scientists.
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Frequent Contacts:
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?USP scientific liaison
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?Reference Standards Evaluation Staff
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?Documentary Standards Division Staff
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?Quality Assurance Staff
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?Applied Compendial Research Division Staff
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Minimum Requirements:
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Ph.D.with at least 2 years in chemistry, analytical chemistry,pharmacy or related field.
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Master degree with at least 5 years of relevant experiences.
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Knowledge, Skills, Abilities, Training and Experience Requirements:
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?Practical knowledge of chemical principles, theories, and practices, and a working knowledge of common analytical procedures, including skill in calibrating and operating analytical instruments such as spectrophotometers and chromatography equipment. Experience in pharmaceutical and/or biotechnology industry preferred.
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?Takes personal responsibility to ensure work is delivered on time and is the highest possible quality.
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?Strong communication and presentation skills, both verbal and written in English.
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?Strong chromatography knowledge with depth of practical experience on analytical techniques such as HPLC, LC-MS, IC, and GC, GC-MS Experience in xcipient analysis is highly preferred.
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?A good knowledge of GLP/cGMP regulations , ICH/VICH guidelines, and compendial methods. Incumbent must possess detailed knowledge of separation sciences and modern analytical instruments, and must be able to work with others to accomplish project goals.
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?Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment.?
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關(guān)于:美國藥典
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除美國之外,USP標(biāo)準(zhǔn)和標(biāo)準(zhǔn)品在的世界上其他130多個國家也得到廣泛的使用。建立185年以來,這些標(biāo)準(zhǔn)一直服務(wù)于世界各地,確保公眾獲得優(yōu)質(zhì)的藥品。
鑒于中國和亞太地區(qū)其他國家的戰(zhàn)略重要性,USP在上海張江高科技園區(qū)設(shè)立了中華區(qū)總部,并建成了USP在全球的第三個標(biāo)準(zhǔn)品研發(fā)中心實驗室。現(xiàn)公開招聘所述職位,誠邀您的加盟。
應(yīng)聘者請將中英文簡歷、近照、應(yīng)聘職位和期望薪資發(fā)送給我們。
欲了解USP更多詳情,歡迎訪問我們的網(wǎng)站。
The United States Pharmacopoeia(USP)is the official standards-setting authority for all prescription and over-the-counter medicines, dietary supplements, and other healthcare products manufactured and sold in the United States.USP is also a world leader and its reference standards are recognized and used in many other countries outside the United States. These standards have been helping to ensure good pharmaceutical care for people throughout the world for more than 185 years.
For more details about USP, please visit our website.
Attaching great importance to China and Asian Pacific countries, USP is setting up its regional headquarter in Shanghai located in Zhang Jiang Hi-Tech Park.
Currently we are looking for the positions for USP-China.Please indicate the position that you are interested and send us your resume and salary expectation to us.
Please send your bilingual resume to us
請將中英文簡歷發(fā)至所述郵箱:uspchinahr@usp.org。
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作者:丁香人才
編輯:wy2011
