Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
• Receives inquiries from FL, investigate and process the inquiry, get necessary information from other Supply Line (SL) functions, reply to FL. • Receives the elevator /equipment/component orders from FL and books the order into SL
Date Posted:2026-06-04 Country: China Location: LOC3309: No.28 Jiuhuan Road, Hangzhou, Shangcheng District, Zhejiang, China Review MOD negotiation projects technical requirement to provide deviation design proposals. Be responsible for MOD negotiation project technical items clarification . Provide technically
JOB DESCRIPTION: 主要职责/Key Responsibilities： 遵照调试SOP，按时完成产品调试任务和原物料功能性评估。 Finish product optimization task and raw material functional evaluation on time, according to product optimization SOP. 参与产品投诉、生产异常、QI、CAPA等质量事件调查。 Participate in dealing with the investigation of product complaints, production deviation and other quality incidents.