Quality Control Technician, Selution (Second Shift)

Overview

When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care.

Our flagship product, SELUTION, combines pharmaceuticals with a traditional balloon catheter, revolutionizing treatments for coronary and peripheral artery diseases. With four Investigational Device Exemptions (IDEs) approved and actively enrolling patients (Coronary ISR, Coronary De Novo, Peripheral SFA, and Peripheral BTK), Cordis is leading the way in delivering transformative medical solutions.

At Cordis, we’re teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients.

If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you. We are the people behind the people who keep saving lives.

• Location: Irvine, CA - ONSITE ONLY**'
• Second Second Hours - 2:00pm-10:30pm***
  
  
  

The Quality Control (QC) Technician is responsible for reviewing, inspecting, dispositioning, approving, and releasing raw material, labeling, and finished product lots. In addition, the Q.C. Technician will be assigned other duties as directed by the Q.C. 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 Q.C. approvals of selected processes in the clean room manufacturing environment.
• Completing other duties as assigned.
• Coordinating HPLC Testing with Q.A. Chemistry Team
• Pro-active review of Quality relevant procedures (SOPs, Q.I.s, RIRs, and Component Specifications
• Completing other duties as assigned.
  
  
  

Qualifications

• High School diploma or equivalent education, 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
• Ability to read, comprehend and follow written procedures.
• Ability to understand and follow verbal instructions.
• Computer skills using Microsoft applications (Outlook, Word, Excel) and other computer software packages.
• Fluent in English
• Ability to communicate ideas, problems and solutions to quality lead or management.
• Ability to collaborate in a team environment
• Ability to work overtime and/or weekends, according to business need
• Ability to be a back-up for second shift support, if needed
  
  
  

Pay / Compensation

The expected pre-tax pay rate for this position is $24.76 per hr. - $30.88 per hr- hourly non-exempt

Actual pay may fluctuate outside of the range depending on skills, education, experience, job-related knowledge and location.

Benefits: Med Alliance offers a competitive benefits package including:

• 401(k)
• Medical, Dental and Vision Insurance
• Life insurance
• Paid time off