What are the responsibilities and job description for the QC Document Inspector II position at GCM Medical & OEM, Inc.?
QC Document Inspector II
Leland, NC
Job Type
Full-time
Description
SUMMARY
The Document Inspector II compiles and verifies documentation required for shipment of product. This role will be responsible for compiling and submitting First Article Inspection (FAI) data to customers, preparing Certificates of Conformance (C of C) and supporting PPAP documentation when required. Minimal inspection experience is acceptable; training can be provided internally as needed.
Responsibilities also include creating customer specific inspection reports, statistical analysis, and coordinating inspection equipment calibration.
JOB RESPONSIBILITIES:
Establishes and follows visual management rules
Manages files, records, and data using advanced computer software (e.g., Prolink)
Contributes improvement ideas and leads small improvement projects
Mentors and trains lower-level document inspectors
Coordinates and files the results of inspection equipment calibration
Advanced responsibilities include:
Creates customer specific inspection reports
Runs basic statistical analysis using mathematical software (e.g., Minitab)
Compiles basic PPAP document packages
Completes customer surveys
Must be a team player as measured by his/her peers
Performs other related duties assigned
Requirements
REQUIRED
HS Diploma or GED
3 years of experience in a medical or aerospace environment
Solid understanding of technical documentation and able to independently determine compliance to requirements
Expert understanding of relevant QMS documents
Open to constructive feedback from leaders
Keeps work area organized and clean
Able to perform all detailed requirements of Document Inspector I job description:
Reviews inspection records, material certifications, and process certifications for completeness and accuracy.
Creates and signs Certification of Compliance based on review of relevant records.
Enters data into inspection reports and spreadsheets.
Coordinates and records procedure, work instruction, and template changes in the Quality Management System
DESIRED
Associate or bachelor’s degree preferred
Lean six-sigma Yellow Belt preferred