On-site QA

Negotiable

Apply for post

Minimum Education:

undergraduate

Number of Recruits:

2

Experience requirements:

3-5 years

Work area:

山东省青岛市城阳区

Job Responsibilities:

1. Responsible for checking the preparation before production, including equipment cleanliness, material usage, production environment, and operators;

2. Responsible for monitoring the production process, confirming the accurate placement of various status signs, and focusing on key control points of the production process;

3. Responsible for on-site inspection of the completion of production records and other related records;

4. Supervise staff to strictly implement job operation methods, process operation procedures, and other relevant documents. Any behavior that does not comply with GMP can be corrected, and the department head should be informed.

 

Qualifications:

1. Relevant majors such as pharmacy, medicine, chemical engineering, etc., with an associate degree or above;

3. More than 3 years of experience in drug production and quality management, familiar with GMP requirements;

4. Good communication skills.