2022药学专业个人英文简历.docx





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1、2022药学专业个人英文简历药学专业个人英文简历 Basic CVName: nationality: ChinaCurrent location: Guangzhou National: HanExit and Entry: Shaanxi is: 170 cm 63 kgMarital Status: Married Age: 30 years oldTraining Certification: integrity badge:Job search intention and work experiencePersonnel types: ordinary jobPosition: Bi
2、ological Chemical / Pharmaceutical Engineering: Biological Engineering Manager, the Minister of Traditional Chinese Medicine / Western medicine / PharmacistsWork Experience: 6 Title: No TitleJob type: full-time can be reported for duty - two weeksMonthly requirements: 5000 - 8000 hope that the worki
3、ng area: Guangzhou, Shenzhen, ShantouPersonal 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 Xian Pharmaceutical Co., Ltd. as a laboratory director.Work experience in detai
4、l: 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
5、.In April 2004 in February 2022 (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,
6、 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 syst
7、em, 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; fam
8、iliar 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 & D:Responsible for the companys new drug R
9、 & D work. Familiar with the procedures for new drug research and development, familiar with the drug R & DThe requirements of independent general agents to complete the preparation of pharmaceutical information, sorting and reporting. Familiar with the principles of conventional test equipm
10、ent and performance, and operation and maintenance of an independent, has a strong inspection techniques and skills, able to complete the inspection work of the Standing Orders.Familiar with the health food of the procedures and requirements development, responsible for the development of health foo
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