Beschreibung
A global pharmaceutical and medical devices manufacturing company is looking for a Document Control Specialist (German speaking) to support a project in it's Quality Control department.This is a great opportunity to work for a leading blue chip company.
Location: Frankfurt area, Germany
Duration: 5 months +
Role and Responsibilities:
Providing document management support to a project which will harmonise the quality systems and standards between two production sites
Drafting documents for the Quality Control department (SOPs, change controls, raw material specifications and validation protocols)
Reviewing and correcting documents
Requirements:
Experience writing and reviewing documents in a GMP regulated environment for the pharmaceutical industry (either in an industrial or academic setting)
Fluent in German and English