Lead Quality Technician

XLR8 EMSSan Clemente, CA
$26 - $30Onsite

About The Position

The Lead Quality Technician is responsible for performing tests and inspections on products, materials, and processes to ensure they meet established quality standards and specifications. This role supports the quality assurance department in maintaining the quality management system and identifying areas for improvement within the manufacturing process.

Requirements

  • Knowledge of quality control principles and practices, and the ability to read and interpret technical drawings, specifications, and work instructions.
  • Proficiency in using various measuring instruments and testing equipment (e.g., calipers, micrometers, gauges).
  • Strong attention to detail, accuracy, and good documentation and record-keeping skills.
  • Basic data analysis and statistical skills, and the ability to follow instructions and procedures.
  • Good communication and interpersonal skills, with the ability to work independently and as part of a team.
  • Basic computer skills (e.g., Microsoft Office Suite).
  • Must be a U.S. Person per EAR Part 772 and ITAR 120.15
  • High school diploma or equivalent
  • 2-4 years of experience in a quality assurance or quality control role in a manufacturing environment.
  • Strong communication and problem-solving skills.
  • Strong analytical, problem-solving abilities.
  • Proficiency in relevant software applications such as QMS software, Microsoft Office Suite, etc.

Nice To Haves

  • Technical training or certification in quality control or a related field is preferred.
  • Knowledge/Certified in regulatory requirements and industry standards such as IPC-A-610 a plus.

Responsibilities

  • Manages non-conforming materials, specifically RMAs, NCMR, and MRB cabinet, with Program Management, Production, and Quality from receipt to resolution
  • Supports/conducts first article inspections (FAI), in-process checks, and final inspections
  • Support internal audits and train other audit personnel
  • Assist in supplier audits as directed by manager
  • Contributes to the development of processes and procedures
  • Lead training process development and ensure training is completed and documented
  • Assists Quality team in analysis of issues and confirmation of defects, when in question
  • Coordinate Document Control activities
  • Support RMA process in root cause and corrective actions. Works with cross-functional teams to implement corrective and preventive actions (CAPA).
  • Develops documents, work instructions, and procedures as needed
  • Ensures compliance with customer requirements and industry standards (IPC-A-610, J-STD-001, AS9100, ISO 13485).
  • Other various tasks as needed to support company requirements
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