Person in charge of drug (new drug) registration and approval
To be negotiated
Education:
Undergraduate
|
Work experience:
3-5 years
|
Number of positions available:
1
Job Description
Job Responsibilities: Organize and prepare various documents required for drug registration (such as trial data, application files, quality standards, etc.); submit registration applications in compliance with the regulatory requirements of the National Medical Products Administration (NMPA) or international regulatory agencies (e.g., FDA), and track the approval progress; communicate and coordinate with regulatory authorities, address any supplementary comments or objections raised during the registration process, and ensure the smooth advancement of the registration work; be familiar with GLP regulations.
Job Requirements: A bachelor’s degree or higher in pharmacy or a related field is required; at least 3–5 years of experience in the registration of Class I new drugs is required; strong communication skills are also required.
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