Jr. QA Technician/ Engineer - Electronic Assembly

Expanding Horizons
San Jose, CA

Job Description

Job Description

My client has an opening a full-time Jr. level QA Technician/Engineer - Electronic Assembly for its San Jose, CA facility. This is a high-tech design and contract manufacturing services company with facilities in China, India, and San Jose, CA.

General Summary

The Jr. Quality Technician /Engineer develops and manages appropriate quality systems and controls to ensure the high-quality and customer satisfaction of new and existing customer-specified products, as well as their compliance with the specified regulations and standards. Help determine solutions to electronic assembly problems (in collaboration with other staff). Recommend appropriate corrective actions and communicate the actions to company management and sometimes directly to customers.

Specific Duties and Responsibilities

· Responsible for qualification activities for new and existing products. This involves, but is not limited to, stencil, machine program, inspection criteria reviews and approvals.

· Collaborate in the adoption of testing and inspection methodology and documentation for new and existing products per customer specifications.

· Assist in installation and maintain company-provided or approved QC process sampling systems, procedures, equipment, and statistical techniques.

· Recommend revisions of procedures and specifications when appropriate.

· Interface with other engineering departments within the company, customers, and suppliers on quality-related issues.

· Collaborate in the review of work instructions and procedures.

· Facilitate and perform internal audits, especially for annual ISO audits.

· Assure adherence to the Company’s Work Instructions (WIs) and Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. Familiarity with IPC standards, such as IPC-600, IPC-610 is desired.

· Understand relevant security, privacy, and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company.

· Ensure other members of the department follow the QMS, regulations, standards, and procedures.

· Perform other work-related duties as assigned

Position Qualifications

· Associate’s degree , a Life Science, or a related field, with 2+ years of quality engineering or relevant experience, or equivalent combination of education and experience (or BS Degree)

· Familiarity with IPC-600, IPC-610, ISO , and other applicable standards, regulations, and laws desired

· 0 - 3 years of Engineering experience in a manufacturing environment recommended, medical device industry helpful

· Must have experience with Electronic devices and or PCBAs

· Excellent verbal, written, and interpersonal communication skills. Ability to speak Mandarin is a plus.

· Proficiency with MS Word, Excel, and PowerPoint

Working Conditions

· General office, laboratory, and cleanroom environments

· Must be able to read, prepare emails, and produce documents and spreadsheets.

· Must be able to communicate and exchange accurate information with employees at all levels daily.

** This is a long-term need for my client. **

Posted 2025-07-30

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