Quality Control Inspector-2nd Shift

ZipRecruiter; Irvine (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a QC Technician for the 2nd shift to ensure product quality in compliance with stringent standards. This role involves collaboration with Engineering and Manufacturing to enhance product manufacturability and maintain rigorous documentation. If you have a background in medical devices and are passionate about quality assurance, this is a fantastic opportunity to contribute to continuous product development and compliance with GMP/ISO standards. Join a team that values safety and quality, and take your career to the next level in a dynamic environment.

Qualifications

• 3+ years of experience in medical devices or quality.
• Familiarity with cGMP, ISO, and Design Control.

Responsibilities

• Troubleshoot and implement corrective actions to align with Quality System standards.
• Inspect and document incoming components and finished goods.

Skills

Troubleshooting

Product Inspection

Documentation Compliance

Training

Education

Associate’s Degree

Technical Certificate

Job description

Job Description

Job Summary:

The QC Technician – 2nd Shift is responsible for testing, inspecting, and ensuring product quality in alignment with the company’s Quality System and customer requirements. This role involves close collaboration with Engineering, Manufacturing, vendors, and suppliers to support continuous product development, manufacturability improvements, and compliance with GMP/ISO standards. Additionally, the technician will maintain proper documentation and adhere to Design Control procedures.

Shift: 3:00pm - 11:30pm

Pay: Up to $26/hr BOE

Type: Temp to Hire

Key Responsibilities:

1. Quality Systems & Troubleshooting: Troubleshoot and implement corrective actions, ensuring documentation aligns with Quality System standards.
2. Product Inspection: Inspect, test, and document incoming components and finished goods. Collaborate with Engineering and Quality to resolve non-conformances.
3. Product Enhancements & Manufacturability: Contribute to product improvements and support the development of inspection fixtures, measurement systems, and calibration.
4. Documentation & Compliance: Review controlled documents (work instructions, specifications, etc.) and maintain logs for compliance (CAPA, CMR, ASL, etc.).
5. Training & Safety: Train team members as necessary and promote adherence to safety standards.

Qualifications:

1. Education: Associate’s Degree, Technical Certificate, or equivalent experience in the medical device industry or similar fields.
2. Experience: 3+ years in medical devices, operations, or quality. Familiarity with cGMP, ISO, Design Control, and Class II/III devices.