Quality management systems expertise meets regulated life sciences at SCIEX in Concord, Ontario, through an on-site 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 in Vaughan employer: SCIEX
At SCIEX, located in the vibrant community of Concord, Ontario, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their fields. As a Senior Mass Spectrometry Research Scientist, you will have access to cutting-edge technology and resources, along with ample opportunities for professional growth and development. Join us to be part of a team that values creativity and encourages contributions to groundbreaking research initiatives in mass spectrometry applications.
