Second Shift QC Technician — Medical Device Release

Cordis, LLC; Irvine (CA); On-site; USD 43,000 - 54,000; Full time

Job summary

Cordis is seeking a Quality Control Technician (Second shift) in Irvine, CA to review, inspect, and disposition raw materials and labels, and to release finished product lots in a regulated manufacturing setting.

The role involves coordinating HPLC testing, ensuring traceability, and supporting QA/QC management. Candidates should have a high school diploma and 1+ year of related experience.

Qualifications

• High school diploma or equivalent required.
• 1+ year of experience in a medical device or other regulated manufacturing industry, preferred.
• Attention to detail and focus allowing for the identification of discrepancies or anomalies.
• Basic understanding of good manufacturing and good documentation practices.
• Computer skills using Microsoft applications (Outlook, Word, Excel) and other computer software packages.
• Ability to work overtime and/or weekends, according to business needs.
• Ability to be a back-up for second shift support, if needed.
• Ability to lift 10-20 pounds.

Responsibilities

• Inspecting and disposition of raw materials and labels.
• Reviewing of work order documentation prior to product release.
• Preparing non-conformity documentation for material disposition as needed.
• Preparing release documentation and appropriate traceability labeling for incoming materials and product release.
• Providing QC approvals of selected processes in the clean room manufacturing environment.
• Completing other duties as assigned.
• Coordinating HPLC Testing with QA Chemistry Team.
• Pro-active review of Quality relevant procedures (SOPs, Q.I.s, RIRs, and Component Specifications).
• Completing other duties as assigned.

Skills

Attention to detail

GMP knowledge

Overtime flexibility

Second shift backup

Education

High school diploma

Tools

Microsoft Outlook

Microsoft Word

Microsoft Excel

Job description

Cordis is seeking a Quality Control Technician (Second shift) in Irvine, CA to review, inspect, and disposition raw materials and labels, and to release finished product lots in a regulated manufacturing setting.

The role involves coordinating HPLC testing, ensuring traceability, and supporting QA/QC management. Candidates should have a high school diploma and 1+ year of related experience.