Manages the full lifecycle of QMS documents (e.g., SOPs, work instructions, quality manuals, technical drawings, and specifications), controlling revisions, approvals, and distribution.
Ensures all document control processes and the eQMS comply with 21 CFR Part 11 requirements (electronic records/signatures), GDP, and international standards.
Leverages deep knowledge of ISO 9001 and ISO 13485 to actively facilitate audit readiness, providing necessary documentation for QMS, regulatory, and customer audits.
Implements document change requests to ensure alignment with change management procedures and quality improvements.
Controls document revisions, approvals, and distribution processes, ensuring the latest versions are accessible to relevant personnel.
Conducts routine audits of controlled documents and records, leading process improvement initiatives for documentation workflows.




Performs other duties as assigned to support the overall quality objectives of the organization.
Education: Bachelor’s degree or Diploma in Engineering, Quality Assurance or a related field preferred. Equivalent work experience will be considered
Work Experience: 2 to 3 years of experience in document control within an electronics manufacturing or related industry.
Experience serving as a system administrator, superuser, or primary support point of contact for an eQMS platform.
Experience supporting audits and maintaining compliance documentation.
Experience working in an setting regulated by ISO 9001 and associated standards.
Demonstrated experience overseeing or coordinating a corporate Training Program within a regulated environment.

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📌 Quality Technician (Electronics/Medical Devices) (British Columbia)
🏢 Brainpower360
📍 British Columbia