QA Inspector 2 - FQA- Day Shift

Unigen, headquartered in Newark, California, is a trusted partner for businesses seeking to power their next generation of products. Founded in 1991, we've grown into a leading provider of electronics manufacturing services (EMS), offering a comprehensive suite of solutions from design and manufacturing to supply chain management. From advanced memory modules to high-density storage devices, our solutions are engineered to meet the demanding needs of today's technology landscape. Our commitment to quality and innovation ensures that our partners have the tools they need to succeed.

At Unigen, you'll have the opportunity to work on cutting-edge projects and make a real difference. Working at Unigen means you'll be surrounded by other innovative companies, have access to top talent, and be close to world-class resources. We offer competitive compensation and a comprehensive benefits package, including 401(k) matching. This location, combined with our benefits, provides a unique advantage for those looking to thrive in the semiconductor industry.


Job Title: FQA Inspector - Level 2
Job Function: Manufacturing Quality
Reports To: Manager, QE and QA, Unigen HQ, Newark, CA

Job Overview

The Level 2 Final Quality Assurance (FQA) Inspector performs advanced-level inspections on PCBA and box build products, ensuring compliance with regulatory, customer, and internal quality standards. This role involves handling high-complexity inspections, mentoring Level 1 inspectors, participating in root cause analysis, and recommending corrective actions. The Level 2 Inspector works with minimal supervision and plays an active role in continuous process improvement initiatives.

Primary Job Responsibilities

1. Advanced Inspection & Testing

• Perform comprehensive cosmetic, dimensional, functional, and compliance inspections for all product lines, including complex PCBA and box build assemblies.
• Ensure finished product compliance with ISO 9001, ISO 13485, ISO 14001, ESD control procedures, and customer-specific quality requirements.
• Conduct inspections in accordance with IPC-610 Class 2 and Class 3 standards.
• Identify and document nonconforming solder joint defects on PTH and SMT components, and verify repair/rework effectiveness.
• Operate and interpret results from advanced test equipment (e.g., AOI, functional testers, continuity testers, X-ray inspection systems).
• Lead FAI verification for high-priority projects and new product launches.

2. Documentation & Reporting

• Accurately record inspection results in the MRP/QMS systems, ensuring traceability and compliance documentation is complete.
• Review and approve Certificates of Conformance (CoCs), inspection reports, and shipment documentation.
• Maintain detailed inspection records for internal audits, customer audits, and regulatory compliance.

3. Mentorship & Team Support

• Provide on-the-job training to Level 1 inspectors and new hires on inspection techniques, tools, and standards.
• Review and verify inspection results performed by junior inspectors before final approval.
• Support cross-functional teams during nonconformance investigations and root cause analysis.
• Share best practices and actively participate in process improvement initiatives.

4. Equipment & Process Maintenance

• Ensure inspection and test equipment is calibrated, maintained, and functioning optimally.
• Recommend updates to inspection checklists and procedures to improve efficiency and accuracy.
• Identify recurring defects and work with engineering to improve manufacturing process quality.

Required Education & Experience

• High School Diploma or equivalent; Associate's degree in Electronics or Quality Management preferred.
• IPC-A-610 Class 2 & Class 3 certification required.
• Minimum 7 years experience in First Article, In-Process, FQA, or Receiving Inspection in an EMS environment.
• Strong ability to interpret technical drawings, BOMs, MPIs, ECNs, deviations, and specifications.
• Proficiency with inspection tools: microscope, calipers, DMM, AOI, X-ray.
• Experience in MRP/QMS systems and MS Office Suite.
• Knowledge of ISO 9001, ISO 13485, ISO 14001 quality systems.