Description
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