Coord 2, Quality Document Sys Mgmt

Professional
Vernon Hills, IL

Roles & Responsibilities

  • Administer EDMS and LMS (manage users, assign privileges, update training requirements).
  • Ensure accurate preparation, storage, and management of documents (electronic and hard copy).
  • Control document numbering, sorting, filing, and retrieval.
  • Process document changes via EDMS.
  • Provide database navigation and troubleshooting support for EDMS and LMS.
  • Assist managers with training assignments and documentation.
  • Provide documentation and training compliance metrics.
  • Maintain device master documentation and records in line with retention policies.
  • Interface with auditors during quality management system reviews.
  • Drive continuous improvement of change control, documentation control, and training systems.
  • Complete assigned projects to support business imperatives.
  • Perform other duties as assigned.

Experience Required

  • Two years of relevant work experience, preferably in a regulated medical device or pharmaceutical environment.
  • Familiarity with blueprints, standard operating procedures, and documentation systems.

Skills & Certifications

  • Proficiency in Microsoft Office (for generating formal procedures, control logs, and databases).
  • Strong verbal and written communication skills.
  • Effective collaboration and teamwork across business functions.
  • Ability to manage multiple projects and deliver results simultaneously.

Eligibilities & qualifications

  • Preferred: Associate degree.
  • Required: High school diploma or equivalent.
  • Experience in regulated environments (medical device or pharmaceutical) preferred.
Posted 2025-09-16

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