1st Shift Quality Inspector & Process Auditor

Otis Worldwide Corporation; Florence (SC); On-site; USD 25,000 - 34,000; Full time

Job summary

Otis Worldwide Corporation is seeking a Quality Inspector (1st Shift) to join the Quality department within our factory. You will audit in-process production against drawings, perform part inspections, and support containment of nonconformances.

Regular use of inspection tools, software, and equipment is expected. Responsibilities include documenting nonconformances, communicating findings to Quality Engineers for root cause analysis, and assisting in process and equipment validation to ensure

Qualifications

• 2–4 years manufacturing experience using inspection gauges/devices
• Strong communication (verbal and written) and ability to interact with all levels of management and shop floor personnel
• Ability to learn technical information quickly and apply to problems
• Autonomy in task management and basic computer skills (email, MS Office) and blueprint/drawing interpretation

Responsibilities

• Perform process audits within production cells, the warehouse and distribution center to ensure compliance to standard work, safety and quality procedures
• Report identified non-conformances in the audit database and communicate essential information to Quality Engineers for root cause analysis
• Perform part inspection to specified drawings, identifying and communicating any defects or non-conformances
• Perform process and equipment validation such as wire crimp pull testing and torque validation

Skills

Manufacturing experience

Inspection gauges

Communication skills

Autonomy

Computer proficiency

Blueprint interpretation

Tools

Excel

Inspection equipment

Job description

Otis Worldwide Corporation is seeking a Quality Inspector (1st Shift) to join the Quality department within our factory. You will audit in-process production against drawings, perform part inspections, and support containment of nonconformances.

Regular use of inspection tools, software, and equipment is expected. Responsibilities include documenting nonconformances, communicating findings to Quality Engineers for root cause analysis, and assisting in process and equipment validation to ensure