Beschreibung
A global specialised pharmaceutical and medical devices manufacturing company is looking for a QC Specialist (German speaking) to support a documentation harmonisation project between two recently merged production sites.Location: Frankfurt am Main area, Germany
Duration: 5-6 months
Role and Responsibilities:
Harmonising and resolving discrepancies between QC documents from two newly merged production sites (including QC test results, method validation, material specifications and SOPs)
Handling the change control of the documentation utilising TrackWise
Implementing the new electronic documentation management system
Ensuring that all documentation is GMP compliant
Requirements:
University or vocational education in Chemistry, Pharmacy or laboratory work
Fluency in German and English language
Hands on pharmaceutical GMP experience within either a QC/analytical or production environment.
This is a great opportunity to get involved with a growing division of a world leading healthcare company. Apply now for further information.