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QC Technician - Medical Device

Cordis
Posted 2 months ago, valid for 11 days
Location

Irvine, CA, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Selution, in partnership with Cordis, is seeking a Quality Control Technician I to support the development of advanced drug device combination products.
  • The role involves reviewing, inspecting, and approving raw materials and finished products, along with other QC-related duties.
  • Candidates must have a high school diploma and at least 1 year of experience in a regulated manufacturing environment.
  • The position offers a pay rate ranging from $20.63 to $25.65 per hour, depending on qualifications and experience.
  • US work authorization is required, and the company will not consider candidates needing visa sponsorship.
Overview

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.


Responsibilities

The Quality Control Technician I is responsible for reviewing, inspecting, dispositioning, approving, and releasing raw material, labeling, and finished product lots. In addition, the QC Technician will be assigned other duties as directed by the QC Lead or by QA/QC Management.

 

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
  • Proactive review of Quality relevant procedures (SOPs, Q.I.s, RIRs, and Component Specifications
  • Completing other duties as assigned.

Qualifications

Qualifications

  • High School diploma or equivalent education require
  • 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

 

 

Pay / Compensation
The expected pre-tax pay rate for this position is $20.63 – 25.65 hourly. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.



 

 

 

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.




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