1、药学专业大学生英文简历模板英文简历虽然不是每一位求职者都必须准备的，但是多准备一份英文简历总会给面试官一个好印象，下面是药学专业大学生英文简历模板，欢迎阅览!药学专业大学生英文简历模板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 int
2、ention and work experiencePersonnel types: ordinary jobPosition: Biological 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 du
3、ty - two weeksMonthly requirements: 5000 - 8000 hope that the working area: Guangzhou, Shenzhen, ShantouPersonal experience: in October 2022 to June 2023 in Baoji City Drug internship.Nearly 6 years of experience in the work of two companies.From July 2023 to March 2023 Granville St. in Xi'an Ph
4、armaceutical 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 ins
5、pection work. And participate in the entire process of GMP certification.In April 2023 in February 2023 (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 th
6、e 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 Qi
7、nghai 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, an
8、d 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 valid
9、ation, etc.). new drug R & D:Responsible for the company's new drug R & 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, so
10、rting and reporting. Familiar with the principles of conventional test equipment 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 procedure
11、s and requirements development, responsible for the development of health food products based on information and preparation works for the preparation. And is responsible for the outreach. Training:Over the years the company is mainly responsible for the laws and regulations at all levels of personn
12、el, expertise and professional skills training and assessment, the training can be firmly carried out the current situation surrounding the company, making the company at all levels of legal awareness and legal concepts, making professional and technical personnel at all levels of expertise to enhan
13、ce professional skills have been greatly improved, can adapt to changing requirements. ISO14001 certification:January 13, 2023 OIA to obtain ISO14001 certificate. Familiar with the regulatory requirements for environmental management system and the use of guidelines (National Institute of Standards)
14、, familiar with the environmental management system certification process and requirements involved in the formation of the EMS work and the appointment of a corporate environmental management manual, procedures, operating documentation (A management type, technology B), such as technical documents
15、and data, company quality management system is responsible for running the organization, coordination, inspection and assessment work, is responsible for internal audit, management review and other work organizations. Pharmaceutical Packaging:Well-known drug-related brochures and packaging label of
16、the laws and regulations, and familiar with the drug label and packaging design specification of the procedures and requirements, the company responsible for assisting the presentation of drug packaging label design work, is responsible for the design of drug packaging label presentation, and printing the final version before review, proof-reading, monitoring and follow-up work.Edu
