急聘GMP咨询兼职

jianai70 · 发表于 2013-12-20 10:26:58

有点远远了

RTibin · 发表于 2013-12-20 17:42:06

说得不错，有收获，顶一下

办公室装修设计 http://www.peee.cn

Jason · 发表于 2013-12-20 20:45:07

介绍Soltoris ,与Michael, 13661872968

ZL221 · 发表于 2013-12-21 09:10:16

努力学习，好过。

Jason · 发表于 2013-12-21 10:16:44

Jason Liou is Expert in Pharmaceutical Product Development and Good Manufacturing Practices (cGMP, IQ/OQ, CMC, FDA, CFDA, TFDA, EU, etc.)

Expert is a professional to the pharmaceutical and biotechnology industries. His background includes 20 years with Pfizer and Abbott in a variety of positions. In his last assignment at Pfizer, he was manager in pilot Plant/Manufacturing responsible for introduction of new products (both final dose form and the bulk pharmaceutical chemical). This responsibility included technology, manufacturing business planning, and project management. Other responsibilities included technical troubleshooting for Antiviral API & final dose form at contract plants, chemical manufacturing, and central project engineering.

Expert is knowledgeable and up-to-date in current Good Manufacturing Practices (cGMPs), especially as applied to bulk pharmaceutical chemicals and Sterile process products. As a Quality Director in Kanion Pharmaceuticals , Expert led the assessment of bulk raw materials and drug substance suppliers from cGMP, business, management, environmental, and technology perspectives. Quality management of products included capsules,t ablets, coated and uncoated, injectable drugs made by both aseptic process and terminal sterilization, and lyophilized products. Expert can answer detailed questions concerning pharmaceutical products and product development, and parenteral product processing.

Expert also started-up the chemical development function in Egretpharma (Shanghai) This included initiating cGMPs for a contract facility and new group. As a quality manager at Norvartis (Shanghai), he has made several audits of bulk manufacturers, primarily cGMP related.

As Senior Director of CMC in Egretpharma, Expert was responsible for the pilot product troubleshooting (process and analytical methods) and transfer of new products from R&D to pilot plant/manufacturing. Expert has written and reviewed Chemistry, Manufacturing, and Controls (CMC) sections for INDs, ANDAs, and DMFs covering both bulk drug an d final drug products.

Throughout Expert's industrial career (>24 years), all his positions have been involved in process research and development, manufacturing, technology transfer from development to manufacturing and quality management. All these positions involved interfacing between R&D, and Pilot Plant/manufacturing. His skills have been honed in process and product development, transfer of technology, strategic long range focus in planning and facilities, up-to-date knowledge of pharmaceuticals cGMPs (especially as applies to bulk drugs and injected drug product), and management of contract development and manufacturing firms.

守望之云 · 发表于 2013-12-21 10:21:52

时间太紧，文件方方面加紧可以赶出来，希望你们的验证工作做在前面，后面再补的话够呛。硬件是难点。

可亲可爱 · 发表于 2013-12-21 10:27:39

你们单位出钱,让蒲公英论坛组个团去帮助一下.

潘晓明 · 发表于 2013-12-21 10:34:33

可以联系我

小兵 · 发表于 2013-12-21 15:47:05

关注。。

wangjin1023 · 发表于 2013-12-21 15:58:03

点，待遇，工作时间。

yihaoli035 · 发表于 2013-12-21 16:35:33

太远了去不了

zjgxyhg · 发表于 2013-12-22 08:55:26

最新告知：已联系到意向人员，谢谢蒲公英网站，谢谢各位的热心！

巴西木 · 发表于 2013-12-22 10:08:17

希望楼主能找到合适的人员

chenjun1985js · 发表于 2013-12-23 09:11:09

QQ加不了！

xhf123456 · 发表于 2013-12-23 09:31:49

这么短的时间，还是从企业内部挖掘人才比较合适，因为，外聘专家对企业现状不熟悉，短时间内很难改观。

戴坚 · 发表于 2013-12-23 10:58:22

原料药认证简单！！！！！！！！！！！

一丁 · 发表于 2013-12-23 16:01:25

qq加不上，怎么联系呀

小李飞刀 · 发表于 2013-12-24 14:59:52

那个地方？

墨石 · 发表于 2013-12-24 15:55:11

不能加QQ，772969781我的QQ

叶非 · 发表于 2013-12-24 17:38:16

需要什么时候？嘻嘻，俺报名先!

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