Process Validation Engineer with strong technical writing background.
They need to be able to write validation protocols and author reports. Technical writing skills are key because the will be authoring a lot of reports.
Working on the floor, used to working with operations GMP/ Pharma experience
Ability to work off shifts – rotating 1st, 2nd, and 3rd shifts
Duties:
Create, revise, and execute protocols and summary reports supporting the transfer of products.