Demo

Senior Document Control And Training Specialist

Twist Bioscience
California, MO Full Time
POSTED ON 3/26/2025
AVAILABLE BEFORE 4/26/2025

As a key member of the Quality Assurance Team, the Document Control and Training Specialist will be responsible for maintenance and sustainment of the eTwist Electronic Document Management System (EDMS) and Learning Management System (LMS) used within Twist. The position requires daily management of documentation from processing draft to published to assignment of training, oversight of the process and its adherence, and training new users on how to use the systems. High attention to detail and hands-on experience using electronic document control and training processes in an ISO or GxP setting is required.

While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required.

What You’ll Be Doing

Document Control Job Duties :

  • Assist with Document Control administrative tasks in the eTwist documentation management system

Processing new and update change Requests

  • Routing documents for approval
  • Publishing approved documents
  • Periodic review and reconciliation
  • Assist with the development of new documents and revising documentation as needed
  • Training Job Duties :

  • Upload new or updated documents into the LMS eTwist
  • Assign required training to employees
  • Create and manage course quizzes
  • Create, edit, and update course curriculums
  • Ensure the training plans align with eTwist Training
  • Manage historical training records
  • Handle eTwist Training inquiries from end users
  • General Job Duties :

  • Troubleshoot eTwist system issues
  • Maintain and update QMS related documents
  • Quality System Metrics monitoring and reporting
  • eTwist system maintenance, as applicable
  • Departmental projects
  • Support other Quality Systems and projects, as applicable
  • What You’ll Bring to the Team

  • B.S. / B.A. Degree or equivalent experience
  • Minimum 5 years of biotech experience with at least 2 years direct experience in Quality Assurance or Compliance document management
  • Learning Management System knowledge and experience required
  • Electronic Document Management systems experience a plus
  • Strong organizational skills and attention to detail required
  • Ability to multitask in a fast-moving environment
  • Experience in an ISO 13485 and / or 9001 environment is a major plus
  • Experience with Atlassian Confluence is highly desirable
  • Master Control experience a plus
  • J-18808-Ljbffr

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