Engineer II, Manufacturing
Southington, Connecticut
Employer: ICU Medical
Industry:
Salary: Competitive
Job type: Full-Time
Description
Position Summary
The Engineer II, Manufacturing is responsible for supporting manufacturing process improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to support and sustain production. The Engineer II will complete intermediate projects with guidance from more experienced engineers and managers and will gain exposure to some of the complex tasks within the job function and are occasionally directed in several aspects of the work.
This role is based 100% onsite at our Southington, CT manufacturing facility.
Essential Duties & Responsibilities
• Immediate expectations:
o Under the guidance of the Engineering leadership, work to improve performance of manufacturing systems, e.g. OEE improvement (quality, performance and uptime), maintenance needs, and scrap reduction
o Support project timelines and milestones and bring them to completion on time and within budget
o Assist in completion of CAPA tasks and deliverables (Corrective and Preventive)
o Use methodical approach for root cause analysis and propose robust technical solutions
o Process technical expert for a manufacturing production line
o Create and edit documents to support Production
o Support initiatives for continuous process and product improvements
o Conduct independent analysis and develop solutions to problems.
o Develop approaches and designs where precedent usually exists.
o Perform developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design
o Receive general project direction. Solicit input from more experienced engineers.
o Work on special projects as they arise
• Long term expectations:
o Initiate and manage projects with adherence to program-management guidelines
o Develop innovative tool design improvements
o Develop and characterize processes and summarize technical details
o Work with Quality Engineers on qualification activities for new or modified processes and equipment.
o Deliver communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize utility and promote cross-functional collaboration.
Knowledge & Skills
• General understanding of automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
• Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.)
• Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations - preferred
• Proficiency in SolidWorks. Mechanical understanding, tool design experience
• Technical writing competency
• Competent in your domain. Familiar with other areas of domain expertise within the team.
• Has a basic understanding of best practices and a basic to intermediate understanding of engineering discipline
• Awareness of the broader product strategy and contribution to it
• Ability to receive general project direction and solicit input from more experienced engineers.
• Requires the ability to independently make decisions that impact the attainment of project objectives.
Minimum Qualifications, Education & Experience
• Bachelor's degree from an accredited college or university (Engineering or Technology)
• 2-4 years of experience in a relevant role
ICU Medical is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Position Summary
The Engineer II, Manufacturing is responsible for supporting manufacturing process improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to support and sustain production. The Engineer II will complete intermediate projects with guidance from more experienced engineers and managers and will gain exposure to some of the complex tasks within the job function and are occasionally directed in several aspects of the work.
This role is based 100% onsite at our Southington, CT manufacturing facility.
Essential Duties & Responsibilities
• Immediate expectations:
o Under the guidance of the Engineering leadership, work to improve performance of manufacturing systems, e.g. OEE improvement (quality, performance and uptime), maintenance needs, and scrap reduction
o Support project timelines and milestones and bring them to completion on time and within budget
o Assist in completion of CAPA tasks and deliverables (Corrective and Preventive)
o Use methodical approach for root cause analysis and propose robust technical solutions
o Process technical expert for a manufacturing production line
o Create and edit documents to support Production
o Support initiatives for continuous process and product improvements
o Conduct independent analysis and develop solutions to problems.
o Develop approaches and designs where precedent usually exists.
o Perform developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design
o Receive general project direction. Solicit input from more experienced engineers.
o Work on special projects as they arise
• Long term expectations:
o Initiate and manage projects with adherence to program-management guidelines
o Develop innovative tool design improvements
o Develop and characterize processes and summarize technical details
o Work with Quality Engineers on qualification activities for new or modified processes and equipment.
o Deliver communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize utility and promote cross-functional collaboration.
Knowledge & Skills
• General understanding of automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
• Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.)
• Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations - preferred
• Proficiency in SolidWorks. Mechanical understanding, tool design experience
• Technical writing competency
• Competent in your domain. Familiar with other areas of domain expertise within the team.
• Has a basic understanding of best practices and a basic to intermediate understanding of engineering discipline
• Awareness of the broader product strategy and contribution to it
• Ability to receive general project direction and solicit input from more experienced engineers.
• Requires the ability to independently make decisions that impact the attainment of project objectives.
Minimum Qualifications, Education & Experience
• Bachelor's degree from an accredited college or university (Engineering or Technology)
• 2-4 years of experience in a relevant role
ICU Medical is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Created: 2024-08-27
Reference: 24300604
Country: United States
State: Connecticut
City: Southington
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