Quality Control Technician I - First Shift (Medical Devices)

Cordis; Irvine (CA); On-site; USD 29,000 - 36,000; Full time

Job summary

Cordis in Irvine, CA is seeking a Quality Control Technician (first shift) to inspect, disposition, and release raw materials and finished products in a regulated manufacturing environment.

Responsibilities include reviewing work orders, preparing release documentation, coordinating HPLC testing with QA Chemistry, and ensuring traceability and adherence to GMP/QbD practices. Candidates should have a high school diploma and 1+ year in a medical device setting.

Qualifications

• 1+ year of experience in a medical device or regulated manufacturing industry
• Attention to detail and focus to identify discrepancies
• Basic understanding of GMP and good documentation practices
• Proficient with Microsoft Office applications
• Ability to work overtime and/or weekends as needed
• Ability to lift 10–20 pounds

Responsibilities

• Inspecting and disposition of raw materials and labels
• Reviewing 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
• Coordinating HPLC testing with QA Chemistry Team
• Proactive review of quality-relevant procedures (SOPs, Q.I.s, RIRs, and component specifications)
• Completing other duties as assigned

Skills

Attention to detail

Good documentation practices

MS Office proficiency

Overtime/weekend flexibility

Able to lift 10-20 pounds

Education

High School diploma or equivalent

Tools

Microsoft Outlook

Microsoft Word

Microsoft Excel

Job description

Cordis in Irvine, CA is seeking a Quality Control Technician (first shift) to inspect, disposition, and release raw materials and finished products in a regulated manufacturing environment.

Responsibilities include reviewing work orders, preparing release documentation, coordinating HPLC testing with QA Chemistry, and ensuring traceability and adherence to GMP/QbD practices. Candidates should have a high school diploma and 1+ year in a medical device setting.