Join Us
On-site QA
Experience Requirements:
unlimited
Number of recruits:
4
Minimum education:
undergraduate
Work area:
江苏省常州市新北区
Job responsibilities:
1、Responsible for the supervision and inspection of the company's production site;.
2、Audit the audit of production records and auxiliary records;.
3、Responsible for supervising the sampling of intermediate and finished products.
4、Responsible for the production of toxic seed distribution and supervision of the destruction of the work after use.
5, batch inspection records, production records collection, audit, organisation.
6、Production and QC electronic data audit supervision and collation.
7, to assist the department manager to complete the daily supervision and inspection of the relevant administrative departments.
Job requirements:
1, bachelor degree or above, pharmaceutical or biological related majors;.
2、Familiar with GMP knowledge, more than 1 year experience in sterile drug production.
3、QC experience is preferred
Welfare treatment:
1、Double holiday, five days a week eight hours work.
2、Provide market competitive salary, salary negotiable.
3、Company in accordance with national regulations for employees to buy social insurance, housing fund.
4, paid holidays (national holidays, annual leave, marriage leave, maternity leave and other paid holidays).
5、Professional training is organised regularly.
Position benefits:
Five insurance, double weekends, regular medical check-ups
