2nd Shift Quality Technician

ClearPath MedicalClearPath MedicalTustin, California, United States
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Posted

9/28/2026

Employment

Full time

Range

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Work style

On-site

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AI summary

Core responsibilities

The Quality Technician performs incoming, in-process, and final inspections to ensure products meet FDA and customer requirements. They are also responsible for maintaining documentation, coordinating calibration activities, and following all safety and quality standard operating procedures.

Requirements overview

Candidates must have at least a high school diploma or GED, with a preference for an associate degree in electronics or mechanics. Proficiency in using measurement tools, basic computer skills, and knowledge of IPC standards are required.

Key skills

Quality assuranceIncoming inspectionIn-process inspectionFinal inspectionFirst article inspectionPreventive maintenanceCalibrationMeasurement toolsMicrometersCalipersExcelTechnical documentationIPC 610IPC 620J-STD standardsAttention to detail

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Education requirements

high schoolassociate degreeprofessional certificate

About ClearPath Medical

Industry

Medical Equipment Manufacturing

Employees

26

Type

Privately Held

Size

51-200 employees

ClearPath Medical is an experienced custom engineering and manufacturing company of high-quality medical interconnect systems for Diagnostic, Therapeutic, and Surgical medical device applications. These interconnect systems include custom cable assemblies, connectors, and electronic interfaces. Located in Tustin, CA, where we design, develop, and manufacture. ClearPath Medical is FDA-registered and ISO-13485 certified. Interested in learning more about ClearPath Medical and its opportunities? Send us a message. We look forward to connecting! www.clearpathmedical.com info@clearpathmedical.com

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Job categories

ManufacturingHealthcareEngineering

Description

Job Summary The Quality Technician, under minimum supervision, shall perform quality assurance activities such as incoming inspection, in-process inspection, and final inspection. Shift: 2nd Shift (2:00 PM-10:30 PM, Monday-Friday) Essential Functions Follow all employee guidelines and Quality System requirements as defined by ClearPath Medicals practices, policies and Standard Operating Procedures to ensure customer and FDA requirements are met. Demonstrate knowledge and act in accordance with ClearPath Medicals Employee Guidelines and applicable quality standards as outlined in ClearPath Medicals Quality Manual. Perform incoming inspection activities, including first article inspection. Perform in-process inspection, including periodic audits of manufacturing work-in-process. Perform final inspection and release, including review of paperwork to ensure that all required inspections and traceability have been documented. Coordinate preventive maintenance and calibration activities. Accurately record process documentation. Must be able to thoroughly interpret, read and follow all work instructions, assembly drawings and other manufacturing/test documentation. Perform other duties as assigned. Must comply with all safety requirements. Required Education Required: Minimum High School diploma or GED. Preferred: Two-year degree (Associates or technical certification) in electronics/advanced mechanics or an equivalent combination of education and relevant work experience in medical devices within a QSR/FDA regulated environment. Required Skills Basic measurement skills using a variety of hand tools and electronic equipment such as rulers, scales, micrometers, calipers, and similar items. General computer skills, including Excel spreadsheets. Simple math skills, including understanding of fractions, cross multiplication, and calculator use. Must be able to work in a fast-paced work environment while performing quality duties. Excellent hand and eye coordination. Excellent attendance and a positive attitude. Good written and oral communication skills; must have the ability to communicate effectively and project a professional image when giving and taking information in writing and in person. Ability to follow verbal and written instructions. Good analytical skills including the ability to identify potential problems. Attention to detail. Capable of both communicating and understanding the English language. Working knowledge of IPC 610, IPC 620, and J-STD standards. Required Experience Previous quality experience in electro-mechanical assemblies and/or other medical devices is desired but not required.

Requirements

  • •Quality assurance
  • •Incoming inspection
  • •In-process inspection
  • •Final inspection
  • •First article inspection
  • •Preventive maintenance
  • •Calibration
  • •Measurement tools
  • •Micrometers
  • •Calipers
  • •Excel
  • •Technical documentation
  • •IPC 610
  • •IPC 620
  • •J-STD standards
  • •Attention to detail

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