Quality Tech II - Medical Device Incoming Inspection

Techtronic Industries - TTI; Anderson (SC); On-site; USD 42,000 - 62,000; Full time

Job summary

Techtronic Industries - TTI Anderson is seeking a Quality Inspector to support FDA and ISO 13485 requirements for incoming part inspection and documentation. The role collaborates with Manufacturing and Supply Chain and requires daily interactions with staff and middle management.

Responsibilities include inspecting and releasing purchased parts, handling nonconforming parts, reviewing Device History Records, and participating in in-process reviews.

Qualifications

• 2-4 years of quality inspection experience.
• High School Diploma or equivalent. Additional college level courses towards an Associates or Bachelor’s Degree is a plus.
• Candidate must be detail-oriented, dependable, and trustworthy; works well as part of a team.
• Knowledge of MS Office, including MS Excel, MS Word, and MS PowerPoint.
• Excellent communication skills: able to read and understand technical reports, specifications, and communicate clearly with the customer.

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

Communication skills

Team player

Reading technical reports

Education

High School Diploma

Associates or Bachelor’s Degree considered

Tools

MS Office

MS Excel

MS Word

MS PowerPoint

Job description

Techtronic Industries - TTI Anderson is seeking a Quality Inspector to support FDA and ISO 13485 requirements for incoming part inspection and documentation. The role collaborates with Manufacturing and Supply Chain and requires daily interactions with staff and middle management.

Responsibilities include inspecting and releasing purchased parts, handling nonconforming parts, reviewing Device History Records, and participating in in-process reviews.