Overview

MedAlliance, 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. MedAlliance is headquartered in Switzerland, with offices in Germany, Singapore, UK and the United States (Irvine, CA).

If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then this is the place for you. Join us, and let’s improve the wellbeing of millions, together.

We are the people behind the people who keep saving lives.

*Location: Irvine, CA - ONSITE ONLY'*

First Shift Hours - 7:00am-3:30pm

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.

• Preferable 2 years of experience in a medical device or other regulated manufacturing

• 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

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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Job Locations US-CA-Irvine

ID 2024-3012

Category Quality/Regulatory

Position Type Regular Full-Time

CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact GlobalHR@Cordis.com