At the University of Pittsburgh, I work as a technical writing consultant. When I started, my main focus was documenting IT process integrations for the Department of Philanthropic and Alumni Engagement. However, as my role evolved, it became clear that there was a larger need—not just to write integration documentation but also to develop a document management system to organize and control an expanding collection of technical documents. Recognizing this gap, I recommended implementing a Quality Management System framework to streamline documentation processes. To address this, I proposed several key initiatives as essential operational milestones:
- Develop and Create Initial Set of PAE Technical Documents (Work Instructions) and associated QSD documents (Quality Manual, Records, Forms, Templates).
- Establish SharePoint Documentation Management System (DMS) - Build a scalable QSD Documentation Management System using our internal SharePoint assets as a Document Management Solution (DMS).
- Implement a QMS Framework for Management of PAE Technical Documentation - Support the implementation of a scalable documentation framework based on a "specialized adoption" of QMS (Quality Management System) standards, guidelines, and principles.
Duties and Responsibilities
In this role, I perform the following duties:
- Manage Document Control: Oversee the control of all Quality Management System (QMS) documents, including policies, procedures, work instructions, forms, and records.
- Create and Revise Documents: Collaborate with departments to create, update, and review QMS documents to reflect process changes, standards, and regulations.
- Ensure Compliance: Ensure QMS documentation complies with quality standards, industry regulations, and legal requirements, staying updated on changes.
- Distribute Documents: Manage document distribution to ensure accessibility, version control, and removal of obsolete documents.
- Coordinate Training and Awareness: Coordinate training programs and awareness campaigns to educate employees on the importance and use of QMS documentation.
- Maintain Records: Manage records related to quality management, such as customer complaints, corrective actions, audits, and inspections.
- Facilitate Document Retrieval: Establish efficient systems for retrieving QMS documents, especially during audits, inspections, or inquiries.
- Support Audits and Inspections: Assist in QMS audits and inspections by providing access to relevant documentation and addressing findings.
- Drive Continuous Improvement: Identify and implement process improvements within the QMS documentation management process.
- Implement Change Control: Implement a change control process to manage changes to QMS documents effectively.
- Mitigate Risks: Assess and mitigate risks associated with QMS documentation processes.
- Foster Communication and Collaboration: Collaborate with various stakeholders to align QMS documentation with business goals.
- Track Documentation Metrics: Track and report KPIs related to QMS documentation management.
- Provide Documentation Training: Provide guidance and training on effective QMS documentation management.
QMS Documentation Dimensions and Hierarchy
The QMS documentation can be represented as a hierarchy, as shown in this diagram.
What is QMS Documentation?
QMS documentation consists of various types of documents that outline the policies, procedures, and records necessary to implement and maintain a quality management system. This documentation can include, but is not limited to:
- Quality Policy: A statement of the organization’s commitment to quality and its goals for achieving customer satisfaction.
- Quality Manual: A high-level document that describes the structure of the QMS, including its scope, processes, and interaction of key elements.
- Procedures: Detailed instructions on how specific activities and processes are to be carried out.
- Work Instructions: Step-by-step guides for performing specific tasks or operations.
- Quality Plans: Documents outlining how quality will be managed for specific projects or products.
- Records: Evidence that processes have been followed and objectives have been met.
Ready to Elevate Your Quality Standards For Doucmentation?
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