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英文簡(jiǎn)歷

藥學(xué)專(zhuān)業(yè)英文簡(jiǎn)歷

時(shí)間:2022-10-07 12:04:51 英文簡(jiǎn)歷 我要投稿
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藥學(xué)專(zhuān)業(yè)英文簡(jiǎn)歷模板

Basic CV
Name: xxx nationality: China
Current location: Guangzhou National: Han
Exit and Entry: Shaanxi is: 170 cm ? 63 kg
Marital Status: Married Age: 30 years old
Training Certification: integrity badge:
Job search intention and work experience
Personnel types: ordinary job ?
Position: Biological Chemical / Pharmaceutical Engineering: Biological Engineering Manager, the Minister of Traditional Chinese Medicine / Western medicine / Pharmacists
Work Experience: 6 Title: No Title
Job type: full-time can be reported for duty - two weeks
Monthly requirements: 5000 - 8000 hope that the working area: Guangzhou, Shenzhen, Shantou
Personal experience: in October 2001 to June 2002 in Baoji City Drug internship.
Nearly 6 years of experience in the work of two companies.
From July 2002 to March 2004 Granville St. in Xi'an Pharmaceutical Co., Ltd. as a laboratory director.
Work experience in detail:
★ laboratory system (the system, technical documentation) of the planning, set up and perfect the work; testing equipment research, selection, procurement, inspection, testing, etc.;
★ laboratory the day-to-day management and inspection work. And participate in the entire process of GMP certification.
In April 2004 in February 2008 (letter into Pharmaceutical Group) Qi Ying Han and Tibetan Qinghai Biological Pharmaceutical Co., Ltd. as the quality manager.
Work experience in detail:
★ Professional Certification:
Familiar with the drugs, food, health food-related laws and regulations, with medicines, food, health food certification procedures and requirements to participate in the company 3 times (6 formulations 12 varieties) GMP certification, certification of health food products 1 ((letter into Pharmaceutical Group) in Qinghai Tinospora health food Co., Ltd.), set up a quality management system, specify the quality of the management of the corresponding documents and materials (raw materials, auxiliary materials, packaging materials), semi-finished product quality standards and criteria for inspection procedures, and designated quality control personnel and the duties of inspectors; familiar with the GMP certification to verify the procedures and requirements involved in the verification (cleaning validation, environmental disinfection cleaning validation, system validation, equipment validation, process validation, etc.).
★ new drug R
Hard hard-working, self-learning ability;
Has a strong team spirit and a strong affinity;
Honest and trustworthy, diligent and responsible.

Personal Contact

藥學(xué)專(zhuān)業(yè)英文簡(jiǎn)歷模板

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