Quality Control Technician I – Medical Devices

Cordis; Irvine (CA); On-site; USD 28,419 - 35,335; Full time

Job summary

Cordis is hiring for a Quality Control/Manufacturing support role in Irvine, CA. The incumbent will inspect materials, review documentation, and prepare release and traceability labeling for incoming materials and product release.

They will also provide QC approvals in the clean room and coordinate HPLC testing with QA Chemistry. Applicants should have a high school diploma or equivalent and at least one year in a regulated manufacturing setting; familiarity with GMP and good documentation

Qualifications

• Requires a high school diploma or equivalent.
• 1 year of experience in a medical device or regulated manufacturing setting preferred.
• Strong attention to detail with the ability to identify discrepancies.
• Basic understanding of good manufacturing and good documentation practices.
• Proficient with Microsoft Office (Outlook, Word, Excel) and related software.

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.
• Coordinate HPLC testing with QA Chemistry Team.
• Review SOPs, QIs, RIRs, and component specifications.

Skills

Attention to detail

GMP knowledge

Overtime availability

Second shift backup

Education

High school diploma or equivalent

Tools

Microsoft Office

Job description

Cordis is hiring for a Quality Control/Manufacturing support role in Irvine, CA. The incumbent will inspect materials, review documentation, and prepare release and traceability labeling for incoming materials and product release.

They will also provide QC approvals in the clean room and coordinate HPLC testing with QA Chemistry. Applicants should have a high school diploma or equivalent and at least one year in a regulated manufacturing setting; familiarity with GMP and good documentation