Quality Documentation Coordinator

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: