Document Control Editor – QA & Regulatory

Abbott Laboratories

Northern (KY)

Hybrid

USD 61,000 - 123,000

Full time

7 days ago
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Job summary

Abbott Laboratories in Abbott Park, IL is hiring a Document Editor within the Quality and Regulatory division. You will ensure changes to controlled documents are justified and properly approved by responsible functions.

The role requires 5–7 years in manufacturing, QA, or documentation control, and a High School Diploma (Bachelor’s preferred). Mastery of Microsoft Office and document management systems is valued.

Qualifications

  • High School Diploma required.
  • 5-7 years experience in manufacturing, QA, or documentation control.
  • Relevant Quality & Compliance business experience.
  • Documentation experience related to policies, processes and procedures.

Responsibilities

  • Support the document change control process ensuring changes are appropriate, justified, and properly approved by responsible functional areas.
  • Primary contact to divisions for controlled document content, format, and change record requirements.
  • Provide direction and leadership for the implementation of document management and archival systems.
  • Provide direction for the use of the Document Management System (DMS) and planned improvements.
  • Manage various divisional departmental projects and document turn around times.
  • Interact with executive management to facilitate change record package approvals.
  • Initiate and execute projects to improve the overall effectiveness of the Document Control department.
  • Support LMS administration and management of the Quality System Training Program.
  • Provides SME on the learning process including learning management system to other functional areas.

Skills

Documentation control
Quality & Compliance
Project management
Communication

Education

Bachelor's degree in Science, IT, Business or Engineering
High School Diploma

Tools

Microsoft Office

Job description

Abbott Laboratories in Abbott Park, IL is hiring a Document Editor within the Quality and Regulatory division. You will ensure changes to controlled documents are justified and properly approved by responsible functions.

The role requires 5–7 years in manufacturing, QA, or documentation control, and a High School Diploma (Bachelor’s preferred). Mastery of Microsoft Office and document management systems is valued.

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