Documentation and Process Improvement Expert (f/m/d) for Pharmaceuticals

Für unseren Kunden aus der Life Sciences Branche suchen wir kurzfristig einen Experten (w/m/d) für die Verbesserungen im Bereich Prozesse und Dokumentation.

Hintergrund:
The overall project goal is to bring the QC department into a steady state of operation. Creation of the Department was established in late 2019 and was asked to within quick succession to not only create new process and procedures but in parallel start performing the Routine daily work. Normally the creation of processes and procedures would be in place close to the beginning of routine production work. To allow the QC to become the fully functional department it needs to become many SOPs, Worksheets, and Job Aids will need to be created. In addition, there is a backlog of updates needed for existing SOPs that will require ownership and assistance.

Aufgaben:
The requirement for this project is that, you will own the process of helping create, send for review (internal and other associated departments), obtain approval of the document, and ultimately have the Documents become Effective and Active within our GMP systems. This is not only a Project Management job; it will require active participation in the full document Update/Creation Process.