Document Control Specialist I

The Document Control Specialist I is responsible for administration of the Change Order (CO) process, compliance with the FDA's Quality System Regulation (QSR), and timely processing and release of new and changed controlled documents. The role requires excellent organizational and communication skills, and experience in a GMP and/or ISO regulated environment.

Requirements

• Minimum one year of professional experience in a GMP and/or ISO regulated environment
• Familiarity with various PC-Based viewing systems
• Proficient with Microsoft Office products
• Previous document control experience
• Medical device, Pharmaceutical and/or Biotech experience
• Proficient with various PC-Based CAD systems