Quality Assurance Specialist - Document Control

location_onRockaway, New Jersey, United Statesschedule3 days ago
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Job description

Summary of Position

  • Implement and adhere to document control procedures, including version control, document approval, and archiving
  • Create and Edit Documents: Prepare, format, and edit documentation related to product development, quality assurance, and manufacturing processes.
  • Coordinate Reviews: Facilitate the review and approval process for new or revised documents by coordinating with relevant departments or stakeholders
  • Assisting in the development and implementation of the Document Change Requests for the company’s-controlled documentation.
  • Assisting with the deployment of training materials to the company's employees and maintaining resulting training records.
  • Other Quality related functions that may be assigned

Primary Job Responsibilities

  • Assist with the initiation and execution of Document Change Requests for the release of new or revised Controlled Documents with respective departmental personnel; maintain DCR and Document Master and Locations specific files in accordance with established policies and procedures.
  • Assist in drafting and reviewing new and revised documents, including but not limited to, policies, procedures, Work Instructions, and related Controlled Documents.
  • Assist with the scheduling and execution of employee training with respective department / function management by reviewing and maintaining training plans and records for new hires and current employees.
  • Communicate with various departments to gather and disseminate information related to documentation needs.
  • Support Teams: Provide support to Quality Assurance, Regulatory Affairs, Engineering and Production teams by ensuring that they have access to the necessary documentation
  • Other duties as may be assigned by manager.

Skills mentioned


Biotech, Medical Devices
Rockaway, New Jersey, United States

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