Job Information
Cordis Manufacturing Engineering Technician, Selution (Second Shift) in Irvine, California
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.
The 2nd shift Manufacturing Engineering Technician* will be responsible for the aiding in the development, evaluation, and optimization of manufacturing processes and methods, utilizing knowledge of product design, materials, fabrication processes, tooling, equipment, and quality control standards.
*2nd Shift 2:00p.m. - 10:30p.m.
Responsibilities
Assist in the development of highly capable manufacturing processes for existing products in manufacturing. Ensure robust transition from product development through full rate production ensuring process stabilization.
Develop, and qualify new tooling and equipment.
Verification and validation of processes, machines, and equipment to meet requirements of Company procedures. IQ/OQ/PQ protocols.
Troubleshoot product/process related issues, perform root cause analysis to develop and implement corrective and preventative action plans.
Qualifications
HS diploma or GED and 1 - 2 years related work experience in the medical device or pharmaceutical field, orAssociates Degree and equivalent work experience.
Strong verbal and written communication skills with ability to effectively communicate at multiple levels in the organization
Strong organization and follow-up skills, as well as attention to detail
Ability to make independent decisions
Knowledge of Validation verification process, Gage R&R, and a clear understanding of FDA's QSR and GMP
Proficiency in Solid works and Computer-Aided Design
Strong analytical, problem solving, and project management skills
Fluent in English
Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA, and other federal, state, and local standards, including meeting qualitative and/or quantitative productivity standards
Light office work
Must be able to lift and carry up to 25 lbs.
Pay / Compensation
The expected pre-tax pay rate for this position is $43,000 – $58,000
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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Job Locations US-CA-Irvine
ID 2024-3113
Category Manufacturing
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