Quality Assurance - Product Inspector in Stanton

Job Summary

The primary responsibility of the Product Inspector I is to conduct sampling and inspection of all materials, components, finished products, and closures utilized in the manufacturing process. These activities must adhere rigorously to established quality assurance programs and approved procedures, including compliance with raw material specifications. Schedule is Tuesday–Friday, 9:30 AM – 6:00 PM
Saturday, 5:00 AM – 1:30 PM

• Examine finished product samples using established methodologies, including comparison against master standards, dimensional measurement, and functional testing.
• Review blueprints and specifications to ensure manufactured products comply with design requirements.

• Ensure the assembly line rigorously adheres to all established SOPs (standard operating procedures), policies, and regulatory/legal requirements.
• Monitor production equipment for safety compliance and immediately remove any non-compliant or hazardous machinery from service.
• Document findings following each inspection, specifying necessary rework and scrapped material, and accurately inputting data into the quality management system.

• Propose and implement process enhancements to optimize production efficiency and elevate final product quality.
• Conduct training for the production team to maintain and reinforce high-quality standards across all operations.
• Maintain the precision of measuring instruments by adhering to the calibration schedule and coordinating necessary repairs.

• Engage in continuous learning and training to remain current with the latest industry knowledge and standards.
• Undertake additional tasks as assigned by management.
• Execute quality audits in accordance with ISO 9001, ISO 13485, FDA regulations, and other relevant standards to maintain compliance.
• Support manufacturing teams by identifying root causes of quality issues and collaborating on corrective actions.
• Maintain detailed records of inspections, measurements, and audit results to support continuous improvement initiatives.

• Proven experience in quality control or quality inspection within manufacturing environments; familiarity with medical device or pharmaceutical industries is a plus.
• Strong knowledge of quality systems such as ISO 9001, ISO 13485, CGMP (Current Good Manufacturing Practice), HACCP (Hazard Analysis Critical Control Point), and FDA regulations.
• Proficiency in using precision measuring instruments including calipers, micrometers, coordinate measuring machines (CMM), and vision inspection systems.
• Ability to perform data collection, analysis, and reporting with high accuracy and attention to detail.
• Experience conducting quality audits and implementing corrective actions to improve product quality.
• Familiarity with calibration procedures for measurement tools like calipers and micrometers.
• Excellent problem-solving skills combined with a proactive approach to maintaining high-quality standards.

Join us in our mission to deliver products that meet the highest safety and quality benchmarks! Your expertise will help shape the future of innovative solutions while ensuring compliance with global standards. We are committed to supporting your growth as a Quality Assurance professional through ongoing training and development opportunities.