Specialist Quality

Requirements

• Process Audit, which includes visual/functional evaluation of product, and verifying production activities are following the control plan, job aids, and ASAS-P.
• Review product and processes to ensure alignment with established quality standards and procedures
• Review and revise quality control procedures as required
• Develop quality training plans to train others as necessary, which partially includes 5S activity
• Maintain Quality Systems record and materials in accordance with Company procedures well as QS/ISO and all relative quality-specific customer
• File and maintain various quality related documents as required
• Prepare quality reports for management and team members as necessary
• Knowledge and understanding of Customer Specific requirements
• Oversee Quality personnel duties including daily product test, data entry, gage set-ups, reproducibility and repeatability audits, “hold tag” administrations, record retention, and calibration
• Schedule and monitor completion of product testing (internal/external) To obtain and/or maintain type approvals for ECE, FMVSS, CCC, In Metro, etc
• Prepare and send out lab samples as needed and required to complete task by due dates
• Maintain and prepare testing records needed for Quality Lab for testing/certifications
• Prepare samples/equipment for DVP&R testing, regulatory audits, and conduct tests
• CMM/Faro Arm Program writing/use
• Maintain & validate Tier 1 product certificates
• Create and provide Quality Training for production
• Assist with functioning retesting when needed.
• Assist with prototype projects.

Benefits

• $1500 Sign-On Bonus
• Medical/Dental/Vision - Day 1
• 401K - 5% match
• 2 weeks' vacation prorated
• Safety shoe & safety glasses program
• Carlex uniform attire