Precision QC Technician – Medical Devices

Cordis; Irvine (CA); On-site; USD 28,000 - 35,000; Full time

Job summary

Cordis in Irvine, CA, seeks a detail-oriented materials QC/designer to inspect and disposition raw materials, review documentation before release, and prepare release and traceability labeling for materials and products. You will support GMP and QA processes in a clean room environment.

Responsibilities include coordinating HPLC testing with QA Chemistry, maintaining non-conformity records, and ensuring adherence to SOPs and specifications. Weekend/overtime availability may be required.

Qualifications

• High School diploma or equivalent required.
• 1+ year of experience in a medical device or regulated manufacturing environment preferred.
• Attention to detail with ability to identify discrepancies.
• Basic understanding of good manufacturing and good documentation practices.
• Computer skills: Outlook, Word, Excel.
• Ability to work overtime and/or weekends as needed.
• Ability to back-up for second shift if required.
• Ability to lift 10–20 pounds.

Responsibilities

• Inspect and disposition of raw materials and labels.
• Review work order documentation prior to product release.
• Prepare non-conformity documentation for material disposition as needed.
• Prepare release documentation and traceability labeling for incoming materials and product release.
• Provide QC approvals of selected processes in the clean room manufacturing environment.
• Complete other duties as assigned.
• Coordinate HPLC testing with QA Chemistry Team.
• Pro-active review of SOPs, QIs, RIRs, and Component Specifications.

Skills

Attention to detail

Good documentation practices

Microsoft Office

Education

High School diploma or equivalent

Tools

Microsoft Office

Job description

Cordis in Irvine, CA, seeks a detail-oriented materials QC/designer to inspect and disposition raw materials, review documentation before release, and prepare release and traceability labeling for materials and products. You will support GMP and QA processes in a clean room environment.

Responsibilities include coordinating HPLC testing with QA Chemistry, maintaining non-conformity records, and ensuring adherence to SOPs and specifications. Weekend/overtime availability may be required.