Recruitment

Check category
Position:
Homepage
/
/
/
Qc Technician

Qc Technician

  • Time of issue:2021-11-17 10:24

(Summary description)

Qc Technician

(Summary description)

  • Categories:Recruitment
  • Author:
  • Origin:
  • Time of issue:2021-11-17 10:24
  • Views:0
Information
The job description Qc Technician
Recruiters Quality inspection department
Hiring
Working place Fengrun District, Tangshan city 
Registered permanent residence requirement There is no limit 
Responsibility According to company requirements for product quality inspection work, the quality inspection department, under the guidance of director of inspection to finished product batch records archive, quarter of raw materials and finished goods, environment and water quality of the data and trend analysis, stability test and fill in the material plan, to ensure that the finished goods inspection report data is accurate and reliable. Responsible for analysis of technical problems of the department. Assist the director in the daily management of the department to ensure the orderly development of the department. Cooperate with related departments for process test, coordinate and arrange related inspection; Search the domestic and foreign frontier inspection technology development status and pharmacopoeia updates, guidelines and other documents. 
Qualification Bachelor degree or above, major in applied chemistry, chemical testing, biology, etc., with relevant working experience.    
Contact
Address: No. 160 park Road, Fengrun District, Tangshan city
By bus: take no. 114, No. 112 and K3 to fengrun District in Tangshan, take no. 108 and no. 109 to fengrun District, transfer no. 106 from the north to the company directly and get off at Shengxue Dacheng Station.
By the end of time 2020-12-31 

 

Scan the QR code to read on your phone

Previous: None
Next: None
Previous: None
Next: None

Relevant information

Hebei Shengxue Dacheng Pharmaceutical(Tangshan) Co.,Ltd.(originally called Thangshan Huaqing Biochemical Pharmaceutical Co.,Ltd., renamed and effected from Dec.2nd ,2007) was granted GMP certificate i
On the morning of May 8, 2019, Chen Shutang, Chief Accountant of CNNC, Zhong Jie, General Manager and Deputy Party Secretary of China Uranium Industry visited Hebei Shengxue Dacheng Pharmaceutical Co., LTD for investigation and guidance.
On May 29, Wang Cheng, General Manager and Deputy Party Secretary of China Uranium Industry Visited Inner Mongolia Shengxue Dacheng Pharmaceutical Co., LTD for investigation. During this period, I listened to the report of the company's production and operation, party building and reform and development, and inspected the production and construction site. Wang Cheng said that In the cruel market competition environment, Shengxue Dacheng has forged a cadre team capable of suffering, dedication and management, especially in the marketization of the bid has made achievements. Wang Cheng stressed that we should adhere to and constantly deepen the concept of innovative development, safe development and green development, integrate into the center, continue to strengthen the party building of the company, find short boards, promote improvement, care for the majority of workers, and actively guide and promote the company's production and operation and project construction, to achieve high quality and high efficiency of the company's development. Guo Qingyin, Deputy chief engineer of China Uranium Industry, Zeng Qingqiang, Director of operation management Department, Liu Tiejun, Party Secretary and Chairman of Hebei Shengxue Dacheng Company and other relevant leaders accompanied the investigation.
In order to fulfill the obligation of environmental protection consciously and accept social supervision actively, we formulate the content of environmental information publicity in accordance with relevant national laws, regulations and standards and in combination with the actual production situation of our company.
Tangshan received the EU-GMP certificate issued by the German government on June 28, 2016, and announced on the official website on July 14, 2016. This is the second time that our company successfully passed the EU-GMP on-site inspection. Eu-gmp certification, the European Medicines Agency (EMEA) certification of the quality management practice for the manufacture of medicines, is a passport for medicines to enter the EU market. Germany is one of the GMP implementation of strict eu member states, represent the global drug administration standards, GMP certificate issued by, is a must for the work of my company's quality management system, is also the height of the company's overall management level of recognition to me, we will be to encourage, constantly improving the quality of individual consciousness, constantly improve the quality management level, keep advantage!

Tel:+86-315-3218811(Outside) 3218833/44(Inside) Fax:0315-3218822