Bilingual Quality Assurance and Management Specialist (Laboratory procedure at Procom
Ottawa, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

19 Nov, 25

Salary

0.0

Posted On

19 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

QUALITY ASSURANCE SPECIALIST (LABORATORY PROCEDURES, QMS), BILINGUAL

The Contractor’s resource will perform tasks in support of this client and other government of Canada departments. The Contractor’s Resource must apply relevant government of Canada policies and information as defined in applicable documents such as codes, standards, specifications, and procedures. You will be analyzing material, such as laboratory procedures and other Quality Management System (QMS) documents to explain the requirement clearly and concisely.
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Tasks include:

  • Writing, modifying, validating and compiling QMS documents.
  • Gathering information, analyzing the subject and the audience, and producing clear QMS documentation.
  • Studying existing material and interviewing Stakeholders.
  • Creating accurate, complete and concise documentation to communicate the needs of the requirement.
  • Assimilating and conveying technical material in a concise, effective manner.
  • Following governmental publishing guidelines.
  • Reviewing QMS documents for conformance to established standards.
  • Design the layout of the QMS documents, guides and manuals.
  • Produce QMS training materials to assist users with the QETE QMS.
  • Assist with quality analysis of trends, patterns, and areas for improvement.
  • Uses word-processing, desk-top publishing and graphics software packages to produce final documents.
  • Store records in the client Records, Document, and Information Management System (RDIMS) produced through the execution of QMS processes according to standard operating procedures.
  • Attend QETE Management Review meetings, take notes and draft meeting records.
Responsibilities
  • Writing, modifying, validating and compiling QMS documents.
  • Gathering information, analyzing the subject and the audience, and producing clear QMS documentation.
  • Studying existing material and interviewing Stakeholders.
  • Creating accurate, complete and concise documentation to communicate the needs of the requirement.
  • Assimilating and conveying technical material in a concise, effective manner.
  • Following governmental publishing guidelines.
  • Reviewing QMS documents for conformance to established standards.
  • Design the layout of the QMS documents, guides and manuals.
  • Produce QMS training materials to assist users with the QETE QMS.
  • Assist with quality analysis of trends, patterns, and areas for improvement.
  • Uses word-processing, desk-top publishing and graphics software packages to produce final documents.
  • Store records in the client Records, Document, and Information Management System (RDIMS) produced through the execution of QMS processes according to standard operating procedures.
  • Attend QETE Management Review meetings, take notes and draft meeting records
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