Medical Device Manufacturer is seeking an experienced Document Control Specialist for their Engineering team.
- Assist in development of procedures to support the manufacturing, quality control, and other Quality Management System (QMS) processes within an ISO 13485 environment.
- Generate and revise items and Bill of Materials (BOMs) in the ERP system
- Support all customer, internal and supplier audits with respect to document control
- Will be responsible for the document control system including: Processing Change Orders, Preparing new and/or maintaining existing documentation and Blueprint review in tandem with the Engineering team.
- Other duties as assigned.