OverviewCordis is a pioneering medical technology company specializing in groundbreaking solutions for cardiovascular and peripheral vascular diseases. 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.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.ResponsibilitiesAssist 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.QualificationsHS 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 organizationStrong organization and follow-up skills, as well as attention to detailAbility to make independent decisionsKnowledge of Validation verification process, Gage R&R, and a clear understanding of FDA's QSR and GMPProficiency in Solid works and Computer-Aided DesignStrong analytical, problem solving, and project management skillsFluent in EnglishAbility 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 standardsLight office workMust be able to lift and carry up to 25 lbs.Pay / CompensationThe expected pre-tax pay rate for this position is $43,000 – $64,000Actual 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.JOIN OUR TALENT COMMUNITYJoining our Talent Community is a great way to receive company news and updates, as well notifications on career opportunities and events that interest you! Please tell us more about yourself so we can align you with future opportunities that match your background, skills and interests.Job Locations US-CA-IrvineID 2024-3113Category ManufacturingPosition Type Regular Full-TimeCORDIS 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