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Sr. Document Control - Medical Device

Sylmar, CA

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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.

Job Requirements


  • High school diploma/equivalent; degree is a plus
  • Minimum of 5 years administrative & document control experience
  • Knowledge of ISO 9001/ISO 13485 compliance
  • Experience working with an ERP 
  • Good communication skills (e.g. verbal and written)
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