Quality management systems expertise meets regulated life sciences at SCIEX in Concord, Ontario, through an in office Quality Systems Specialist role.

This specialist supports SCIEX’s Quality Management System across ISO 9001, ISO 13485, FDA requirements, and internal standards. The position works within Quality Assurance & Regulatory Affairs, reporting to the Senior Manager, QMS. Responsibilities span audits, CAPA, document control, training, eQMS administration, quality metrics, and continuous improvement.

Key Responsibilities:

- Maintain and improve QMS processes and regulatory compliance
- Support audit planning, execution, responses, and action closure
- Administer eQMS documents, records, assignments, and reports
- Guide audit and CAPA owners through investigations
- Monitor metrics, trends, dashboards, and compliance risks

Requirements:

- Bachelor’s degree or equivalent education and experience
- Three years of quality assurance or QMS experience
- Working knowledge of ISO 9001 and ISO 13485
- Experience with audits, CAPA, document control, and records
- Experience with eQMS, procedure writing, and reporting

Apply quality systems, audit, CAPA, and eQMS expertise to strengthen compliance at SCIEX in Concord.

📌 Quality Management Systems Specialist (Vaughan)
🏢 SCIEX
📍 Vaughan