Manufacturing QA Coordinator - Drive Improvement

Essilorluxottica; Sydney; On-site; AUD 90,000 - 120,000; Full time

Benefits offered by this job

$1,500 product allowance

Family & Friends discounts up to 50%

Up to 50% off Oakley eyewear

OneSight Foundation volunteering

Career opportunities across network

Free on-site parking

Job summary

EssilorLuxottica is recruiting a Manufacturing Quality Assurance Coordinator in Silverwater, NSW. You will drive quality systems, perform root-cause analysis and oversee inspection protocols for materials, in-process items and finished lenses. A degree in manufacturing/engineering and QA experience are essential.

Experience with medical devices is advantageous, and a strong eye for detail will support continuous improvement and regulatory compliance in a dynamic production environment.

Qualifications

• Degree in manufacturing or engineering
• Experience in quality engineering or a related field
• Proficiency in quality management systems and QA methodologies
• Medical device knowledge is desirable
• Attention to detail for quality inspections and compliance

Responsibilities

• Implement and maintain quality management systems in line with ISO standards
• Conduct root cause analysis and corrective actions for quality issues
• Monitor production data to identify trends and improvements
• Develop and execute inspection and testing protocols for materials and products
• Create and update inspection plans, SOPs and work instructions
• Maintain records of quality activities and audits
• Present quality metrics to management

Skills

Quality engineering

QA methodologies

Statistical analysis

Education

Bachelor's degree in manufacturing or engineering

Tools

Statistical analysis tools

Job description

EssilorLuxottica is recruiting a Manufacturing Quality Assurance Coordinator in Silverwater, NSW. You will drive quality systems, perform root-cause analysis and oversee inspection protocols for materials, in-process items and finished lenses. A degree in manufacturing/engineering and QA experience are essential.

Experience with medical devices is advantageous, and a strong eye for detail will support continuous improvement and regulatory compliance in a dynamic production environment.