QA Inspector I (Monday to Friday 6:00am to 2:30pm)

Prismatik; Irvine (CA); On-site; USD 26,394 - 31,684; Full time

Job summary

Prismatik is seeking a QA Inspector to ensure the products we ship meet the highest standards. This hands‑on role involves inspecting incoming materials, monitoring production quality, and supporting compliance with our quality systems.

The position requires at least 1 year of QA/QC experience, preferably in a medical device environment. You will be handling material testing, line inspections, and maintaining DHR records in a fast-paced facility.

Qualifications

• Minimum of 1 year in QA/QC; medical device industry preferred.
• Ability to lift up to 40–50 lbs with/without assistance.
• Experience with quality systems and inspections is a plus.

Responsibilities

• Perform incoming receiving inspections of goods.
• Conduct raw material testing to ensure quality.
• Perform RMAs and release of incoming materials and finished goods.
• Carry out in-process, semi-final, and final inspections per drawings.

Skills

QA inspection

Material testing

Documentation (DHR)

Safety procedures

Job description

We’re looking for a QA Inspector to help ensure the products we ship meet the highest standards.

This is a hands‑on role where you’ll inspect incoming materials, monitor production quality, and support compliance with our quality systems.

Shift: M-F 6:00am to 2:30pm

Essential Functions

• Performs incoming receiving goods inspection.
• Conducts raw material testing to ensure product quality.
• Performs return material/product inspection (RMA).
• Authorizes the release of incoming raw materials and finished goods.
• Performs in-process, semi-final, and final inspections according to drawing and specifications.
• Completes inspection records according to procedure(s).
• Conducts line inspections for production and packaging operations.
• Maintains the quarantine area(s) to ensure that all non‑conforming, rejected material, and materials awaiting inspection are clearly labeled with status.
• Maintains, organizes, and ensures files are accurate and complete (i.e. DHR).
• Prioritizes inspection based on manager and demands of manufacturing and research & development.
• Follows all safety guidelines.
• Maintains compliance with quality system procedures and company policies.
• Organizes and maintains SDS binder.
• Performs other related duties and projects as business needs require at direction of management.

Education and Experience

• Minimum of one (1) year of experience in quality assurance/quality control required; experience in a medical device industry preferred.
• Ability to frequently push and/or pull up to forty (40) pounds and up to fifty (50) pounds with assistance and/or use of equipment.
• Ability to frequently lift or carry up to forty (40) pounds and up to fifty (50) pounds with assistance and/or use of equipment.

Pay Range: $19.16-$23.00/hr

Exact compensation may vary based on skills and experience.