כאן תמצאו את ג׳וב החלומות שלכם

The opportunity
The jobholder acts as a member of Teva External Manufacturing and Supply Operations (EMSO).
Jobholder closely interacts with the Team, the CMO Manager and QRM and if required other departments such as Operations, Procurement, Supply Chain, MS&T, and Regulatory Affairs and provides complete support from quality perspective.
The position is to review the QMS documents like change controls, deviations, OOS/OOT, batch records associated with formulations that include various dosage forms of products supplied to EMSO. The market is primarily for US, EU, UK and Canada.  
The jobholder will be responsible for review of QMS documents and ensuring that the supply is not interrupted due to the delay and provides timely updates on the status of the QMS documents. 
 

How you’ll spend your day
Responsible to follow the Quality Management System of EMSO organization, which is relevant to the job function
Review of deviations/OOS/OOT
Management of Global/Regional Projects
Life cycle management of Change control system
Preparation of Standard Operating Procedure 
Training Management
Document Management
Batch record review.