Manufacturing Engineering Technician, Selution (First Shift)
Posted on Sep 17, 2024 by Cordis
Irvine, CA
Retail Trade
Immediate Start
Annual Salary
Full-Time
Overview:
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 1st 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.
*1st Shift 7:00a.m. - 3:30p.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, 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.
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 1st 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.
*1st Shift 7:00a.m. - 3:30p.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, 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.
Reference: 200951949
https://jobs.careeraddict.com/post/95376460
Manufacturing Engineering Technician, Selution (First Shift)
Posted on Sep 17, 2024 by Cordis
Irvine, CA
Retail Trade
Immediate Start
Annual Salary
Full-Time
Overview:
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 1st 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.
*1st Shift 7:00a.m. - 3:30p.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, 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.
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 1st 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.
*1st Shift 7:00a.m. - 3:30p.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, 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.
Reference: 200951949
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