上海招聘

Description
Responsibility:
·Responsible for analytical method development and method validation of NPD projects;
·Responsible for drafting Stability protocol& report and conduct stability study;
·Responsible for the establishment of product specification for raw materials and finished products, draft cleaning validation protocol and report ; responsible for the writing of analytical research section within drug application dossier and provide necessary support for on-site inspection;
·Provide necessary supports for analytical method transfers from R&D centers to manufacturing sites, cooperate closely with AP Analytical Centre, US R&D centers and contract labs;
·Maintain the management system for validation, calibration and preventive maintenance of analytical instruments and equipments in order to ensure proper functioning of analytical instruments and equipments; Ensure the analytical laboratories' compliance with GMP, EHS and other related company policies.
Qualifications

Requirement:
·Bachelor degree or above, Pharmaceutical Analysis or Analytical Chemistry related, Master or Ph.D. degree is preferred;
·Above 3 years of experience in pharmaceutical analytical method development and validation, working under GMP is preferred.

上海强生制药有限公司诚聘