Quality Technician II – Medical Devices QA

TTI Consumer Power Tools, Inc.; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

TTI Techtronic Industries is seeking a detail-oriented Quality Inspector to support FDA and ISO 13485 compliance for incoming parts and documentation. The role interfaces with Quality, Manufacturing, and Supply Chain to ensure compliant parts and proper records for medical devices.

Responsibilities include incoming receipt, inspection, release of purchased parts, nonconforming part handling, device history records review, and collaboration with engineers and assemblers to maintain product

Qualifications

• 2-4 years of quality inspection experience.
• High School Diploma or equivalent; an Associate's or Bachelor's degree is a plus.
• Proficient in MS Office (Excel, Word, PowerPoint).
• Ability to read and interpret technical reports and specifications.
• Must be detail-oriented, dependable, and a team player.

Responsibilities

• Perform incoming receipt, inspection, and release of purchased parts and materials.
• Assist in nonconforming process of defective parts.
• Perform required manufacturing line clearance activities to verify parts and equipment prior to assembly.
• Perform required document review (Device History Record) of medical devices.
• Assist with in-process nonconforming and complaint reviews as assigned.
• Performs other duties as assigned.

Skills

Detail-oriented

Team player

Excellent communication

Education

High School Diploma or equivalent

Associates/Bachelor's degree preferred

Tools

MS Office (Excel, Word, PowerPoint)

SAP experience a plus

Job description

TTI Techtronic Industries is seeking a detail-oriented Quality Inspector to support FDA and ISO 13485 compliance for incoming parts and documentation. The role interfaces with Quality, Manufacturing, and Supply Chain to ensure compliant parts and proper records for medical devices.

Responsibilities include incoming receipt, inspection, release of purchased parts, nonconforming part handling, device history records review, and collaboration with engineers and assemblers to maintain product