QC Inspector Lead

ONE SOURCE MANUFACTURING TECHNOLOGYTX
98d

About The Position

The Lead QC Inspector position at One Source Manufacturing Headquarters in Leander, TX, involves promoting teamwork within the department and across the organization. The role requires working with team members and management to meet daily departmental needs and priorities, serving as the first level of conflict resolution, and providing professional service to all departments. The Lead QC Inspector will ensure that best practices for product verification and job completion are consistently applied. Responsibilities include developing processes and work instructions to improve operations, assisting team members in verifying inspection results, maintaining CMM program files, and using QC equipment and software as needed.

Requirements

  • Minimum of High school diploma.
  • Minimum 5 years of experience in a Manufacturing Quality Control environment.
  • Bachelor's degree in a scientific discipline, ASQ certification, or equivalent experience required.
  • Ability to understand the use of hand held measurement tools.
  • Use and programming of CMM Software (PC DMIS, Modus).
  • Computer skills (Excel, Word, Outlook, Inspection Xpert, Minitab).
  • Attention to details.
  • Work well in a team environment.

Responsibilities

  • Promote an atmosphere of teamwork within department and across OSM.
  • Work with team members and management to achieve 100% of department daily needs and priorities.
  • Perform as the 1st level of conflict resolution, escalate as needed.
  • Provide consistent, thorough, professional service to all departments.
  • Assure best known methods for product verification and job completion are used in the department at all times.
  • Development of processes, work instructions, preventative measures, etc. to improve overall operations.
  • Assist team members in verification of inspection results, including products found to be discrepant.
  • Maintain CMM program files.
  • Use and instruction of all QC equipment and procedures.
  • Use and instruction of NCMR software.
  • Other QC tasks as determined.
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