QA Specialist
To be negotiated
Education:
Undergraduate
|
Work experience:
Unlimited
|
Number of positions available:
2
Job Description
Job Responsibilities: Responsible for drafting and implementing QA inspection plans for GLP and GCP trials, as well as preparing QA inspection reports; responsible for inspecting trial protocols, trial reports, source documents, and the entire trial process.
Job Requirements: Major in pharmacy, toxicology, pharmacology, biology, pharmaceutical sciences, or a related field; English proficiency at Level 6 or above; bachelor’s degree or higher. Familiar with relevant regulations such as the Good Clinical Practice for Non-Clinical Drug Studies, the Good Clinical Practice for Non-Clinical Veterinary Drug Studies, and the National Certification and Accreditation Administration’s Principles of Good Laboratory Practice. Experience in GLP and GCP certification processes is required. QA-related experience is highly desirable.
Salary: To be discussed
Benefits and Perks: Six social insurances and one housing fund, free lunch, shuttle bus, accommodation, employee health check-ups, holiday benefits, birthday gifts, and more.
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Contact phone number
Ms. Li:+86 15760970681
Mr. Su:+86 19991001701
Landline:+86-29-33656828
Company Address
4th Floor, Unit C. Building 9. Small and Medium-sized
Enterprise Park, Airport Industrial Zone Airport New Ciy,Xixian New Area, Shaanxi Province
©2026 Xixian New Area Guorui Yinuo Drug Safety Evaluation and Research Co., Ltd.
WhatsApp：8613940397353
Email：hr-xian@grglp.com
Landline：862933656828
Mr. Su：8619991001701
Ms. Li：8615760970681