About the Role
Overview
Title: Documentation Coordinator II
Job Type: Full-time, permanent
Location: Netherlands (Waalwijk) – On-site
Cpl Life Sciences is collaborating with a growing Medical Device Organisation who are looking to recruit 2x Documentation Coordinator II. These positions are on-site roles, so you must be located close to the site and hold the full right to work.
The Associate Documentation will work under the guidance of the Quality Assurance Manager to maintain the Document Control System to ensure control, security, integrity, and availability of documentation to site personnel. This person is responsible for implementing and maintaining document control and record retention for the site. This person is responsible for the control of documents and coordination of controlled document-related activity pursuant to GMP/ISO regulations.
Responsibilities:
Ready to Join Through a Referral?
Apply now and get connected directly with the hiring team
Apply for this Position