2nd Shift Quality Technician

ClearPath Medical LLC; Tustin (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

ClearPath Medical LLC is seeking a Quality Technician to perform incoming, in-process, and final inspections under minimal supervision. The role requires adhering to Quality System requirements and FDA guidelines, with a focus on documenting inspections and traceability.

The position operates on the 2nd Shift (2:00 PM-10:30 PM, Monday-Friday) and emphasizes attention to detail, accurate measurements, and good communication in a fast-paced medical device environment.

Qualifications

• Must have High School diploma or GED.
• Preferred: Associates degree or technical certification in electronics/advanced mechanics or equivalent in medical devices within a QSR/FDA regulated environment.

Responsibilities

• 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 inspections and traceability.
• Coordinate preventive maintenance and calibration activities.
• Accurately record process documentation.
• Must follow work instructions, assembly drawings and manufacturing/test documents.
• Must comply with all safety requirements.

Skills

Basic measurement skills

Excel

Math skills

Attention to detail

Communication skills

Reading instructions

English language

IPC knowledge

Education

High School diploma or GED

Associates or technical certification in electronics/advanced mechanics

Tools

Calipers

Micrometers

Rulers

Excel

Job 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.