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Welcome to Longevity Valley Pharmaceutical!

Leadding Setter of International Standards for Ganoderma lucidum / Dendrobium Officinale    Stock Symbol:603896

Current position:
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Work area

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Time of issue:

engineer

Jinhua city, zhejiang province | | | | wuyi - -

No limit

2024-12-02

Application
Work area: Jinhua city, zhejiang province | | | | wuyi - - Nature of the work:Full timeGender requirements:No limit Salary: Negotiable

Job Requirements:

Pharmacy or related major, relevant working experience is preferred, familiar with GMP related industry trends, policies and regulations, execution, communication and coordination ability, strong sense of responsibility, team spirit.


Job Responsibilities:

To assist workshop director organize production in accordance with the GMP, internal control system, supervision of production workers in accordance with the provisions of the rules of production technology, equipment, operating procedures, post standard operating procedures for production, participate in the GMP certification, especially the equipment validation, cleaning validation, process validation, etc, the workshop is responsible for production safety, personnel safety and property safety.

 

 

Secretary of the quality assurance

Jinhua city, zhejiang province | | | | wuyi - -

No limit

2024-12-02

Application
Work area: Jinhua city, zhejiang province | | | | wuyi - - Nature of the work:Full timeGender requirements:No limit Salary: Negotiable

Job Requirements:

Pharmacy, food related major, at least 3 years working experience in the same position, familiar with national laws and regulations of food, health food, medicine and other products as well as GMP system, can skillfully use computer office software.
 

Job Responsibilities:

Responsible for the preparation of the company's GMP certification self-inspection plans, regularly organize related personnel to implement self-inspection activities; Maintain internal quality management system of the company (including internal inspection, internal audit) and external contact (including coordination of second and third party audit and improvement tracking after audit); Responsible for the preparation, drafting and revision of the quality assurance system documents of drugs, health food, food, etc., copy and distribute the system documents to relevant departments, update and maintain the documents, archive and backup the electronic documents regularly.