IM
Engineer I, Product Design
Accepting applicationsICU Medical · Southington, CT
Full-Time Principal
Posted
1d ago
Category
Verification
Experience
Principal
Country
United States
Job Description
Position Summary
The Engineer I, Product Design position in the Vascular Access Product Engineering team will have the opportunity to manage product design changes for post market product in the medical field while collaborating with Product Design Engineers, Systems Engineers, R&D Testing Labs, Marketing, Design Assurance, as well as internal and external Manufacturing teams. The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is responsible for developing and implementing design and development plans through adherence to established design control processes and good engineering and documentation practices. The position plays a key role in assisting in the supply continuity and compliance challenges involved with medical devices. Familiarity with Minitab and SolidWorks, or comparable statistics and CAD software, is a plus.
Essential Duties & Responsibilities
Organizes, plans, and executes formal design verification activities for small to medium scale design change projects. Supports similar activities for other projects of varying scale.
Writes test protocols, performs test method validations and executes test plans, and authors test reports with data analysis and technical conclusions.
Supports risk management activities through hazard analysis and design failure and effects analysis (DFMEA) and the identification and implementation of risk mitigation.
Supports the analysis and evaluation of solutions to complex problems. Conducts investigations of varying complexity pertaining to the change in designs, methods, materials or processes, and investigates possible applications of the results.
Assists in root cause analysis and the development and implementation of solutions for non-conforming events through the Corrective Actions and Preventable Actions (CAPA) process.
Adheres to established design control processes and good engineering practices
Designs and models components, devices, test fixtures, prototype/pilot tooling for various product lines using SolidWorks
Develops test procedures to ensure specifications and regulations are met
Executes engineering and validation studies on products
Work on special projects as assigned
Knowledge & Skills
Detail oriented and ability to organize large amounts of work and data
Strong interpersonal skills required in the areas of verbal and written communications, customer focus, time management, professionalism, and team building
Excellent project leadership and ability to expedite project completion
Able to review and interpret technical documentation such as engineering drawings and component specifications
SolidWorks competency preferred
Minitab or similar statistics competency preferred
Understanding of engineering mechanics and physics
Able to analyze technical problems, develop creative solutions, and implement effective changes
Familiarity with machine shop practices
Familiarity of drafting standards
Minimum Qualifications, Education & Experience
Must be at least 18 years of age
Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.
Experience in Medical Device Product Development preferred.
Work Environment
This is largely a sedentary role.
This job operates in a professional office environment and routinely uses standard office equipment.
Typically requires travel less than 5% of the time
About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're Ready To Bring You Consistent Quality, Innovation, And Value In More Areas Than Ever. Our Focus Allows Us To Bring You
Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
Significant US IV solutions manufacturing and supply capabilities.
ICU Medical EEO Statement
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants
Show more Show less
Position Summary
The Engineer I, Product Design position in the Vascular Access Product Engineering team will have the opportunity to manage product design changes for post market product in the medical field while collaborating with Product Design Engineers, Systems Engineers, R&D Testing Labs, Marketing, Design Assurance, as well as internal and external Manufacturing teams. The primary focus of this role will be supporting the post market development and performing design verification of medical device components and products of varying complexity. The engineer is responsible for developing and implementing design and development plans through adherence to established design control processes and good engineering and documentation practices. The position plays a key role in assisting in the supply continuity and compliance challenges involved with medical devices. Familiarity with Minitab and SolidWorks, or comparable statistics and CAD software, is a plus.
Essential Duties & Responsibilities
Organizes, plans, and executes formal design verification activities for small to medium scale design change projects. Supports similar activities for other projects of varying scale.
Writes test protocols, performs test method validations and executes test plans, and authors test reports with data analysis and technical conclusions.
Supports risk management activities through hazard analysis and design failure and effects analysis (DFMEA) and the identification and implementation of risk mitigation.
Supports the analysis and evaluation of solutions to complex problems. Conducts investigations of varying complexity pertaining to the change in designs, methods, materials or processes, and investigates possible applications of the results.
Assists in root cause analysis and the development and implementation of solutions for non-conforming events through the Corrective Actions and Preventable Actions (CAPA) process.
Adheres to established design control processes and good engineering practices
Designs and models components, devices, test fixtures, prototype/pilot tooling for various product lines using SolidWorks
Develops test procedures to ensure specifications and regulations are met
Executes engineering and validation studies on products
Work on special projects as assigned
Knowledge & Skills
Detail oriented and ability to organize large amounts of work and data
Strong interpersonal skills required in the areas of verbal and written communications, customer focus, time management, professionalism, and team building
Excellent project leadership and ability to expedite project completion
Able to review and interpret technical documentation such as engineering drawings and component specifications
SolidWorks competency preferred
Minitab or similar statistics competency preferred
Understanding of engineering mechanics and physics
Able to analyze technical problems, develop creative solutions, and implement effective changes
Familiarity with machine shop practices
Familiarity of drafting standards
Minimum Qualifications, Education & Experience
Must be at least 18 years of age
Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.
Experience in Medical Device Product Development preferred.
Work Environment
This is largely a sedentary role.
This job operates in a professional office environment and routinely uses standard office equipment.
Typically requires travel less than 5% of the time
About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're Ready To Bring You Consistent Quality, Innovation, And Value In More Areas Than Ever. Our Focus Allows Us To Bring You
Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
Significant US IV solutions manufacturing and supply capabilities.
ICU Medical EEO Statement
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants
Show more Show less