This role provides support for document control processes and other related quality systems within a growing medical device manufacturer
Job Summary
This role provides support for document control processes and other related quality systems within a growing medical device manufacturer.
Responsibilities include supporting change control, part number management, BOMs, and applying revision control within PLM and ERP systems.
The Document Control Administrator will review changes for accuracy and completeness, contribute to improvement initiatives, and support the organization and archiving of controlled documents.
Matching Summary
This role provides support for document control processes and other related quality systems within a growing medical device manufacturer.
Skills & Requirements
Must-have
Product Lifecycle Management (PLM) systems
Enterprise Resource Planning (ERP) systems
Change control administration
Part number management
BOM structure management
Revision control application
Nice-to-have
Collaborative problem solving approach
Proactive customer interface
Good Documentation Practices guidance
Key Requirements
Manufacturing company experience required
Familiarity with GDP and medical device field preferred
Familiarity with ISO 9000 and/or ISO 13485 preferred