Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Lead Document Controller to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
Responsibilities:
Responsible for leading and coordinating document control processes within the project and the various phases (Engineering documents).
Manage the engineering registry in different systems to allow accurate and easy retrieval of information for the project engineering team, ability to locate information in a timely manner and accurately is a key function of the role
Reproduction of information into both printed and electronic format for communication to the engineering team
Manage and coordinate with Engineering providers and...