Job Responsibilities:

1. Responsible for the investigation of stability samples and the maintenance and maintenance of the stability box;

2. Responsible for the management of QC laboratory standards;

3. Responsible for OOS, deviation and change of each group of QC;

4. Responsible for HPLC/GC/IR/stability chamber/TOC/UV/polarimeter data backup and HPLC audit trail;

5. Responsible for the review of all inspection records and instrument usage records of each group of QC;

6. Responsible for the review of work standard product re-standard report, preparation verification plan and report;

7. Responsible for the preparation of the verification plan, original records and reports, and record the verification ledger;

8. Responsible for the development and verification of new product analysis methods;

9. Responsible for personnel training and performance appraisal of each group;

job requirements:

1. More than five years of work experience, participated in official GMP certification, familiar with GMP regulations, FDA and COS certification experience is preferred;

2. Bachelor degree or above, major in pharmacy, pharmaceutical engineering, chemistry, etc.;

3. Have good communication, cooperation and coordination skills;

4. Able to guide and train lower-level employees to do relevant inspection work;

Work location: No. 5, Donghai Fourth Avenue, Toumen Port Economic Development Zone, Zhejiang Province

Please call: 0576-85589365 E-mail:hr@ausunpharm.net