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

Jobbeschreibung

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.

Must have skills
GLP/ GMP

Startdatum
Frühestens: sofort
Spätestens: 9. Nov 2020
Idealerweise ist ein kurzfristiger Projektstart möglich.

Laufzeit
12 Monate
12 Monate mit Option auf Verlängerung

Auslastung
Vollzeit
Verfügbarkeit in Vollzeit gewünscht, mindestens 4,5 Tage/Woche

Remote
Teilweise möglich
To be discussed

Erforderliche Sprachkenntnisse
Englisch, Deutsch
Fließend Deutsch und Englisch ist Voraussetzung

Budget
75-115€ pro Stunde
Bitte Remote + Onsite-Stundensatz angeben.
inkl. Uplink-Gebühr

Einsatzorte
30938 Burgwedel