GCM

Document Inspector II

GCM  •  Leland, NC (Onsite)  •  3 months ago
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Job Description

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
GCM

About GCM

GCM leads the medtech industry in meeting the extensive manufacturing requirements of the most challenging, tight tolerance components and assemblies in the world today. We offer a full range of solutions from product design optimization, design for manufacturing, advanced materials selection, metrology expertise, up to full scale mass production capabilities. We support the major OEM’s in the highly complex areas of surgical robotics, genomics, drug delivery, aerospace and others – Customers who require the need to push the technical envelope are a perfect fit for GCM’s design and technical capabilities.

At the core of GCM is our highly technical, seasoned engineering and development team servicing global customers from our worldwide ISO13485 manufacturing facilities in Silicon Valley CA, Chicago, Wilmington NC and Dongguan China. Our 400,000+ sq ft of manufacturing space is equipped with the most advanced 5-axis machining, robotics, sheet metal, robotic welding, screw machining, EDM and other supporting capabilities in the industry today. Each of our factories are centered around our extensive metrology facilities at each location. GCM also has the capability for large footprint machining and fabrication of precision, complex components.

GCM is successful through a collaborative approach to engineering, ideal for forward moving customers who require excellence in product realization and has well positioned itself to help customers beyond manufacturing who value GCM as a true extension of their company.

Industry
Manufacturing & Production
Company Size
51-200 employees
Headquarters
Union City, CA
Year Founded
1978
Website
gogcm.com
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