Manufacturing Engineering Technician, Selution (Second Shift) - Cordis

Cordis 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.

• 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.

• HS diploma or GED and 1 - 2 years related work experience in the medical device or pharmaceutical field, or
  Associates 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 – $64,000
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.