Quality Control Technician (First Shift)
About The Position
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. The Quality Control (QC) Technician (first shift) 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. 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.
Requirements
- 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
- Ability to lift 10-20 pounds
- US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
501-1,000 employees
