重慶藥友制藥有限責(zé)任公司是由上海復(fù)興醫(yī)藥控股集化學(xué)

1、重慶藥友制藥有限責(zé)任公司，是由上海復(fù)興醫(yī)藥控股、集化學(xué)藥物制劑、化學(xué)原料藥和中藥制劑的研發(fā)、生產(chǎn)、銷售于一體的現(xiàn)代化高新技術(shù)企業(yè)。經(jīng)過(guò)六十多年的不懈努力和追求，現(xiàn)已發(fā)展成為總資產(chǎn)、年銷售收入逾4億元，年利稅總額近億元的質(zhì)量效益型企業(yè)，建成了國(guó)際一流、全國(guó)生產(chǎn)規(guī)模最大的凍干制劑生產(chǎn)線，以阿拓莫蘭、炎琥寧為代表的凍干產(chǎn)品占有同類產(chǎn)品市場(chǎng)的主導(dǎo)地位，形成了藥友產(chǎn)品品牌和企業(yè)品牌的精品效應(yīng)，使藥友更具高科技、高水準(zhǔn)、專業(yè)化的核心競(jìng)爭(zhēng)力,成為符合GMP規(guī)范、國(guó)內(nèi)一流的現(xiàn)代化的制藥生產(chǎn)基地，實(shí)現(xiàn)了跨越式的發(fā)展，是中國(guó)醫(yī)藥綜合競(jìng)爭(zhēng)力最強(qiáng)的企業(yè)之一，中國(guó)西部醫(yī)藥的代表。藥友產(chǎn)品涉及消化、心血管、抗生素、營(yíng)養(yǎng)、

2、抗腫瘤等多個(gè)治療領(lǐng)域，而且都實(shí)現(xiàn)了GMP整體認(rèn)證，部分產(chǎn)品正在申請(qǐng)歐洲 EDQM 和美國(guó) FDA 認(rèn)證?，F(xiàn)代化的辦公大樓，高標(biāo)準(zhǔn)的生產(chǎn)廠房，健全的質(zhì)量保證和控制體系，科學(xué)嚴(yán)謹(jǐn)?shù)纳a(chǎn)管理，世界一流的制藥設(shè)備和檢測(cè)儀器，先進(jìn)的計(jì)算機(jī)網(wǎng)絡(luò)控制平臺(tái)，健全的售后服務(wù)和信息反饋系統(tǒng)，有效地保證物料從進(jìn)廠、生產(chǎn)、銷售等全過(guò)程均處于受控狀態(tài)，確保牌產(chǎn)品更加安全穩(wěn)定、迅速有效，產(chǎn)品質(zhì)量市場(chǎng)抽檢合格率長(zhǎng)期保持100%。藥友堅(jiān)持走產(chǎn)學(xué)研聯(lián)合之路，不僅有自己的科研機(jī)構(gòu)，而且在與國(guó)內(nèi)多家科研院所和大專院校建立聯(lián)合實(shí)驗(yàn)室的同時(shí)，還與許多科研院所建立了廣泛聯(lián)系，并同美國(guó)獨(dú)資的重慶科美納米生物技術(shù)有限公司合作，成立了重慶科美

3、藥友納米生物技術(shù)開發(fā)有限公司，形成了較好的企業(yè)技術(shù)創(chuàng)新網(wǎng)絡(luò)，共同研發(fā)具有自主知識(shí)產(chǎn)權(quán)的新藥，以不斷提高企業(yè)的產(chǎn)品創(chuàng)新水平和市場(chǎng)競(jìng)爭(zhēng)能力。近年來(lái)，藥友制藥近二十個(gè)產(chǎn)品分別獲得國(guó)家和重慶市高新技術(shù)產(chǎn)品證書?！拔覀児餐瑩肀Ы】怠钡慕?jīng)營(yíng)理念，引領(lǐng)藥友不斷研制更多安全有效的藥品，為臨床用藥和患者健康帶來(lái)福音；“誠(chéng)實(shí)守信，互惠共贏”的商業(yè)原則，使藥友與商業(yè)客戶攜手共進(jìn)，構(gòu)筑了強(qiáng)大的市場(chǎng)營(yíng)銷網(wǎng)絡(luò)；堅(jiān)持走國(guó)際化道路，與美國(guó)、德國(guó)、日本、吉爾吉斯斯坦、越南、巴基斯坦、馬來(lái)西亞等國(guó)醫(yī)藥同行建立長(zhǎng)期合作關(guān)系，使藥友制藥成為社會(huì)大眾廣泛認(rèn)同和喜愛的優(yōu)秀企業(yè)。Chongqing Yaoyou Pharmaceutica

4、ls Co., Ltd is a hi-technical enterprise developing, producing and selling chemical preparation, drugs made of chemical materials and Chinese drugs. After 60 years of unremitting efforts and relentless pursuit, it has become benefit and quality enterprise. Now, total assets and annual sales revenue

5、exceed 400 million RMB with the annual pre-tax profit total of nearly 100 million RMB. It has established international first-rate production line of lyophilized preparation of the largest scale of production in China. The lyophilized products such as Reduced Glutathione for Injection and Potassium

6、Sodium Pehydroandroandrographolide Succinate play a leading part in the market share of the similar products. The brand effect of Yaoyou products and the enterprise let Yaoyou have core competition of high technology, high quality and specialization, becoming the national first-rate pharmaceuticals

7、production base answering for the standard of GMP. Realizing leapfrog development, it is one of Chinese pharmaceutical plants with the strongest overall competitiveness, the delegate of western pharmaceutical plants.The productions of Yaoyou cover with digestion, cardiovascular disease, antibiotic,

8、nutrition, anticancer. And all the manufacturing lines of Yaoyou have passed GMP certification by SFDA. Yaoyou is preparing CTD dossiers of some products for COS of EDQM (E.U.) and ANDA of FDA (U.S.A) as well as applying for cGMP Audit. Modern office block, high-quality work shop, sound quality assu

9、rance system and control system, reasonable production management, world first-rate pharmaceutical equipments and inspection instruments, advanced control platform of computer network and sound maintenance service and feedback system ensure that the whole process of materials entry into factory, pro

10、duction to distribution has been controlled, which ensure the products of Yaoyou safer and more effective, with the outgoing qualified rate of product quality keeps 100% for a long term.Yaoyou adheres to the development pattern of combining production, study and research. Yaoyou has its own R &

11、D institute and founds united laboratories with many scientific research institutions and colleges in China and establishes extensive contact with a lot of scientific research institutions. Besides, cooperating with Chongqing COMED NANOPHARMA CO., LTD exclusively with American investment, Yaoyou est

12、ablishes Chongqing COMED YAOYOU NANOPHARMA CO.,LTD, forming good enterprise technology innovation network, researching and developing the new medicine with self-owned intellectual property right to ceaselessly boost the innovation level of its products and sharpen it competitive edge. Recently, abou

13、t 20 kinds of products produced by Yaoyou have been praised with the certificates for national hi-tech product and Chongqing hi-tech product. Management concept of “l(fā)ets all embrace the health” leads Yaoyou to develop more secure and effective pharmaceuticals to satisfy patients need in relentless p

14、ursuit of meeting the requirements of customers, staff and shareholders. The business principle of “honesty and faithfulness, mutual benefit and win-win” lets Yaoyou develop with customers to build strong marketing network. Adhering to Globalization, Yaoyou establishes a long business term with phar

15、maceutical confreres in America, Germany, Japan, Kirghizstan, Vietnam, Pakistan, Malaysia, etc, which makes Yaoyou as the excellent enterprise identified by and popular with the public.地址：重慶市渝北區(qū)人和鎮(zhèn)星光大道100號(hào) 郵編：401121電話：0086118 聯(lián)系人：鄒小姐電子郵箱：zouhyAddress：No. 100Xingguang Avenue, Renhe Town

16、, Yubei Disrect, Chongqing City China(New High-Tech park, New Northern Zone)Post: 401121Tel: 0086118 call Helen ZouE-mail: zouhy1. Title: Director of ANDA Formulation DevelopmentJob DescriptionThis position will lead a group of pharmaceutical research scientists, working on the formula

17、tion development of ANDA projects. It is a full-time job position located in Chongqing, China.Responsibilitiesl Establish a team of ANDA formulation development and the corresponding management system.l Manage the formulation screening for ANDA projects.l Lead a team conducting ANDA formulation rese

18、arch projects.l Coordinate the production of Bio-batch.l Prepare the formulation development documents for ANDA registration.Qualificationsl Ph.D degree or equivalent.l 10 years of experience in U.S. pharmaceutical industry; 3 years of experience in leading generic drug development projects.l Experi

19、ence in generic drugs/CMC, injectables based research and development is highly desirable. l Experience in preparing quality research documentation for FDA requirements.l Strong ability in communication, leadership, and teamwork.l Proficiency in both English and Chinese.2. Title: Director of ANDA Qu

20、ality ControlJob DescriptionThis position will lead a group of pharmaceutical research scientists, working on quality control of ANDA projects. It is a full-time job position located in Chongqing, China.Responsibilitiesl Establish an ANDA quality analysis team and quality control management system.l

21、 Manage the screening of equipment and material required by the projects.l Lead a team to conduct quality analysis required by ANDA projects, such us quality specification, analysis methods, stability programs.l Prepare the quality research documents for ANDA registration.Qualificationsl Ph.D degree

22、 or equivalent.l 10 years of experience in an U.S. pharmaceutical industry, 5 years of experience in quality control projects for drug development.l Experience in quality research of pharmaceutical formulations; Experience in quality research of injectable formulation is highly desirable.l Knowledge

23、 and experience of required documentation and presentation.l Strong ability in communication, leadership, and teamwork.l Proficiency in both English and Chinese.3. Title: Director of cGMP Quality AssuranceJob DescriptionThis position will lead a group of staff, working on quality assurance of cGMP p

24、rojects. It is a full-time job position located in Chongqing, China.Responsibilitiesl Set up a cGMP project team and a systematic working plan.l Lead a team to conduct quality assurance work and gap analysis of cGMP projects.l Specify the quality requirement for Bio-batch/Validation batch/commercial

25、 batch.l Manage the audit and selection on suppliers of API and other material.Qualificationsl M.S. degree or equivalent.l 10 years of experience in an U.S. pharmaceutical manufacturer, 5 years of experience in quality management for drug development.l Experience in receiving FDA inspections.l Exper

26、ience in quality management of generic drugs manufacturing required; Experience in sterilized injectable manufacturing is highly desirable. l Strong ability in communication, leadership, and teamwork.l Proficiency in both English and Chinese.4. Title：Senior Consultant on cGMP Job DescriptionThis pos

27、ition will be engaged in consulting and supervising on cGMP projects. It is a full-time job position located in Chongqing, China.Responsibilitiesl Provide consultation on cGMP inspection/ improvement and advice on regulatory affairs.l Communicate regularly with the officials of FDA regarding ANDA pr

28、ojects. l Assist the set up of cGMP project and advance the process. Coordinate the collaboration between the multidisciplinary teams of ANDA projects.l Review the registration documents prepared by ANDA teams.l Foresee, analyze and help mitigate risks associated with the ANDA projects.Qualification

29、sl 20 years of experiences in U.S. pharmaceutical industry, and 10 years experiences in generic drugs research and production (retirees acceptable). l Familiar with FDA regulations on quality management and product registration.l Familiar with FDA requirements for sterile Injectable products is high

30、ly desirable.l Strong ability in communicating with FDA officials.l Experience in preparing documents to meet FDA requirements.l Strong ability in communication, leadership, and teamwork.1 職位名稱：ANDA 項(xiàng)目配方研發(fā)總監(jiān)職位描述：這個(gè)崗位將帶領(lǐng)一組研究人員，負(fù)責(zé)開發(fā)ANDA項(xiàng)目的配方研究。該職位是全職工作，工作地點(diǎn)位于中國(guó)的重慶市。主要職責(zé)：l 建立ANDA項(xiàng)目配方研究的工作團(tuán)隊(duì)；建立配方研究項(xiàng)目的管理體系；l 負(fù)責(zé)項(xiàng)目配方篩選的管理；l 領(lǐng)導(dǎo)團(tuán)隊(duì)按計(jì)劃完成ANDA配方研究項(xiàng)目；l 協(xié)調(diào)完成Bio-batch 生產(chǎn)；l 負(fù)責(zé)編寫ANDA 注冊(cè)文件中的配方部分。職位要求：l Ph.D學(xué)位l 在美國(guó)制藥企業(yè)、 研發(fā)機(jī)構(gòu)的相關(guān)領(lǐng)域工作10年以上；從事仿制藥研發(fā)3年以上；l 有仿制藥配方研究/CMC經(jīng)驗(yàn)，有注射劑研究經(jīng)驗(yàn)優(yōu)先；l 具有ANDA文件編寫經(jīng)驗(yàn)；l 良好的溝通能力，有團(tuán)隊(duì)領(lǐng)導(dǎo)能力及合作精神；l 熟練使用中、英兩種語(yǔ)言2 職位名稱：ANDA 項(xiàng)