Number of Recruits:
1.Mainly responsible for supervising and ensuring the implementation of GMP;
2.Supervise the implementation of process discipline and various process parameters during the production process;
3.Participate in the development of a validation master plan and conduct drug production validation.
1.College degree or above,major in Chemical engineering,biopharmaceutics,animal husbandry and veterinary medicine,etc;
2.Familiar with GMP,with at least two years of experience in quality management or production management in pharmaceutical companies;
3.Have good communication and coordination skills and certain management skills,proficient in using office computers.