BS in Chemical or Biomedical Engineering. Two years process improvement engineering or validation engineering experience in the pharmaceutical or medical device industry, including cGMP, CAPA process, Change Control, Risk Assessment Tools FMEA. Two years experience in qualification process for equipment, facilitiesutilities, including authoring and execution of protocols and reports. Two years experience on practical use of six sigma tools DOE, Root Cause Analysis, Statistical Process controls for process improvement and investigations.

Categories: eb3

0 Comments

Leave a Reply

Avatar placeholder

Your email address will not be published. Required fields are marked *