Quality System Coordinator

Overview

Employment Type:

Temp-to-Perm, fully onsite

About the Role

Seeking a detail-oriented Quality Systems Coordinator to support and maintain quality management systems in a fast-paced manufacturing environment. This is a fully onsite, temp-to-perm opportunity with competitive pay. The ideal candidate will have hands-on experience with ISO 13485 and a strong understanding of regulated quality systems.

• Maintain and update quality system documentation, including SOPs, work instructions, and forms.
• Support internal and external audits, ensuring compliance with ISO 13485 standards.
• Track and manage corrective and preventive actions (CAPAs), nonconformance reports (NCRs), and quality metrics.
• Assist in quality management system (QMS) process improvements and continuous improvement initiatives.
• Collaborate with cross-functional teams including Manufacturing, Engineering, and Regulatory Affairs to ensure adherence to quality standards.
• Support training and onboarding related to quality processes and documentation.

• Experience with ISO 13485 required.
• Knowledge of QMS processes, CAPA management, audits, and document control.
• Strong attention to detail and organizational skills.
• Excellent communication skills and ability to work collaboratively onsite.
• Previous experience in a medical device or regulated manufacturing environment preferred.

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act
• Los Angeles City Fair Chance Ordinance
• Los Angeles County Fair Chance Ordinance for Employers