Document Management & QA Support Coordinator

Sotera Health Company

Ottawa

On-site

CAD 60,000 - 85,000

Full time

8 days ago

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Sotera Health Company is seeking a Document Management & QA Support Coordinator to join the on-site Ottawa team. The role supports drawing releases, engineering changes and configuration management within the Quality function, ensuring documentation accuracy and proper control across the QMS.

You will work with Engineering and Quality to manage controlled documents, use MasterControl and PDM tools, conduct audits, and maintain regulatory records.

Qualifications

  • Post-secondary education in Engineering Technology, Records and Information Management, Quality, Business Administration or a related discipline.
  • 3-5 years of experience supporting configuration management, drawing control, engineering change management, and Product Data Management (PDM).
  • Experience with electronic document management systems (QMS and/or PDM).
  • Experience supporting engineering documentation, controlled drawings, bills of materials and engineering changes.
  • Experience in manufacturing, technical or regulated environments.
  • Familiarity with ISO 9001/ISO 13485/ISO/IEC 17025 or CSA N299 quality systems is an asset.
  • Experience conducting audits and managing QMS metrics is a strong asset.

Responsibilities

  • Ensure engineering documents, drawings, product structures and related documentation meet quality and configuration management requirements prior to release.
  • Review and verify accuracy of engineering drawings, BOMs and configuration information using PDM systems.
  • Support engineering change activities, new product introductions and updates through document/control processes.
  • Manage creation, revision, approval and distribution of controlled documents using electronic document management systems.
  • Troubleshoot document and configuration-related issues and support users with document management workflows.
  • Maintain quality and regulatory records per requirements.
  • Support QA activities including audits and maintenance of QMS metrics and databases.
  • Maintain and trend quality-related data and prepare routine reports.

Skills

Attention to detail
Analytical skills
Problem solving
Organizational skills
Communication skills
Collaboration

Education

Engineering Technology / Records & Information Management / Quality / Business Administration

Tools

MasterControl
Autodesk Vault
PDM systems

Job description

## Document Management & QA Support CoordinatorApply: On-site: Ottawa - ON: Full time: Posted Yesterday: R-2026-1129The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health.Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies. **The Document Management & QA Support Coordinator, reporting to the Director Quality, reviews and verifies that engineering drawings, bills of material, and configuration management meet internal requirements.****Working within the Quality function and closely with Engineering, the role supports drawing releases, engineering changes, and configuration management process to ensure technical information is accurate, current, traceable, and properly controlled.** **The position also supports document management and broader QA activities within the Quality Management System (QMS), including the control and maintenance of documents within MasterControl.** **Key Responsibilities*** Ensure engineering documents, drawings, product structures and related documentation meet established quality and configuration management requirements prior to release.* Utilize Product Data Management (PDM) systems to review and ensure accuracy of engineering drawings, bills of material and configuration-related information.* Support engineering change activities, new product introductions and product updates through effective document and configuration control.* Manage the creation, revision, approval and distribution of controlled documents using electronic document management systems.* Troubleshoot document and configuration-related issues and support users with document management and workflow processes.* Maintain quality and regulatory records in accordance with established requirements.* Support Quality activities including document reviews, complete internal and supplier audits, maintenance of quality databases and reporting activities.* Maintain and trend quality-related data and prepare routine reports and metrics. **Qualifications**Post-secondary education in Engineering Technology, Records and Information Management, Quality, Business Administration or a related discipline. 3-5 years of experience supporting configuration management, drawing control, engineering change management, and Product Data Management (PDM) within a manufacturing or engineering environment.Experience working with electronic document management systems (eg Quality Management Systems and/or Product Data Management systems.)Experience supporting engineering documentation, controlled drawings, bills of material and engineering change processes.Experience in a manufacturing, technical or regulated environment.Familiarity with ISO 9001, ISO 13485, ISO/IEC 17025 or CSA N299 quality systems is an asset.Experience conducting audits and managing QMS metrics is a strong asset. **Skills and Competencies**Strong attention to detail and commitment to the accuracy and integrity of drawings and configuration information.Ability to work independently, manage competing priorities, and make sound decisions within established requirements.Confidence to ask challenging questions, identify inconsistencies, and escalate concerns when information or requirements are unclear.Strong analytical, problem-solving, organizational, and communication skills.Ability to collaborate effectively with key stakeholders.Advanced proficiency with Microsoft Word, (formatting and maintaining complex documents).Experience with MasterControl, Autodesk Vault or similar document/PDM systems is essential.
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Document Management & QA Support Coordinator
Document Management & QA Support Coordinator

Canadian Inclusion • Ottawa

On-site
CAD 60,000 - 90,000
Document Management & QA Support Coordinator
Document Management & QA Support Coordinator

Nordion • Ottawa

On-site
CAD 60,000 - 75,000
Document Management & QA Support Coordinator
Document Management & QA Support Coordinator

Nordion (Canada) Inc. • Ottawa

On-site
CAD 60,000 - 75,000
Quality Management System (QMS)
Quality Management System (QMS)

CS GROUP - Canada • Montreal

Hybrid
CAD 90,000 - 120,000
Hybrid Work
Medical Insurance
Dental Insurance
+4
Senior QMS / Quality Engineer ( Medical Devices)
Senior QMS / Quality Engineer ( Medical Devices)

Avenue39, Inc. • Mississauga

On-site
CAD 90,000 - 130,000
Spécialiste des systèmes de qualité/Quality Systems Specialist
Spécialiste des systèmes de qualité/Quality Systems Specialist

Fresenius Medical Care • Vaudreuil-Dorion

On-site
CAD 65,000 - 85,000
Quality and Regulatory Specialist
Quality and Regulatory Specialist

Cloud DX, Inc. • Kitchener

On-site
CAD 70,000 - 90,000
Technical Writer (Pharmaceutical Engineering Contractor)
Technical Writer (Pharmaceutical Engineering Contractor)

GMP Engineering Inc. • Oakville

On-site
CAD 55,000 - 96,000
Document Control Team Lead
Document Control Team Lead

AtkinsRéalis Group • Montreal

Hybrid
CAD 85,000 - 120,000
Senior Quality Assurance Specialist - Consultant
Senior Quality Assurance Specialist - Consultant

Value Apothecaries • Canada

On-site
CAD 90,000 - 120,000