Company Overview

GCM is a leading outsourced manufacturer of high-precision components and assemblies, providing an integrated platform of manufacturing solutions primarily for the MedTech industry, as well as select Diversified Industrial end markets. GCM is backed by Avista Capital Partners, a leading private equity firm focused on growth-oriented healthcare businesses. Within MedTech, the Company manufactures products for high-growth segments such as robotic assisted surgery, radiotherapy, diagnostic technology, and other vital equipment. GCM maintains strong and long-tenured relationships with many market-leading Original Equipment Manufacturers (OEMs) who value the Company's strong capabilities in highly engineered and difficult to manufacture precision components. The Company operates three manufacturing facilities in Silicon Valley, Chicago, and Dongguan, China.

SUMMARY

The Document Inspector II compiles and verifies documentation required for shipment of product. Responsibilities also include creating customer specific inspection reports, statistical analysis, and coordinating inspection equipment calibration.

GENERAL RESPONSIBILITIES

• Must be a team player as measured by his/her peers.
• Open to constructive feedback from leaders
• Keeps work area organized and clean
• Establishes and follows visual management rules
• Manages files, records, and data using advanced computer software (e.g. Prolink)
• Expert understanding of relevant QMS documents

• Solid understanding of technical documentation and able to independently determine compliance to requirements
• Contributes improvement ideas and leads small improvement projects
• Mentors and trains lower-level document inspectors.

DETAILED RESPONSIBILITIES

• 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
• 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

KNOWKEDGE AND SKILL REQUIREMENTS

• HS Diploma with a 2-year degree preferred.
• 3 years’ experience in a medical or aerospace environment.
• Lean six-sigma Yellow Belt preferred

WORKING CONDITIONS

• Typical desktop environment.
• Work may require occasional weekend and/or evening work.