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PROCESSING APPLICATION
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Job Requirements of Manufacturing Engineer I:
-
Employment Type:
Contractor
-
Location:
Skaneateles, NY (Onsite)
Do you meet the requirements for this job?
Manufacturing Engineer I
Careers Integrated Resources Inc
Skaneateles, NY (Onsite)
Contractor
Your Role at Client
This is where your expertise helps people!
You are a problem solver.
Complex projects or unexpected challenges are just opportunities to bring your considerable
abilities to use.
Whether working independently or with a trusted team, you are always ready to tackle a project and work hard to find solutions.
Your talent is needed across a wide variety of industries.
As a Manufacturing Engineer you have a wide array of career choices, but are motivated by the opportunity to work in a company that supports innovation, professional development, and a purposeful mission.
Your Team
We are a team of inquisitive individuals who embrace a collaborative environment to take on sophisticated challenges that meet the needs of our patients.
We often need to change directions and respond to issues to avoid disruptions in our fast-paced manufacturing environment.
Together, we build and maintain a positive work environment. Our team is dedicated to quality.
Delivering life-saving products is about getting them right, and our technical expertise
and experience working in a manufacturing environment empower us to meet that challenge.
When you join us, you will work with a team of committed individuals who trust each other to deliver on the tasks at hand.
We support innovation and out-of-the-box thinking balanced with collaboration across functions and other teams.
Our leadership understands the need for continuous education and provides opportunities for further development.
What You'll Be Doing
Member of cross functional Electronics Gemba Team with responsibility for up to 8
medical device manufacturing assembly lines.
Execute Process and Equipment Validation/Verification Strategies for new or changing manufacturing process elements.
Represent manufacturing on R&D project core teams, responsible for deliverables, collaborating with internal stakeholders and ensuring productivity.
Develop and maintain manufacturing process documentation including but not limited to:
Manufacturing Process Speci fications, Device History Records, Tooling/Equipment Specifications, Preventative Maintenance and Calibration procedures through Engineering
Change Management (ECM) process.
Perform and document root-cause analysis for
Non-Conforming Material Reports.
Summarize and report on departmental Safety, Quality, Delivery, Productivity, and Cost performance measures.
Use Lean/Six Sigma methodology to identify
and drive Continuous Improvement Projects to enhance Safety, Quality, Delivery, Productivity, and Cost performance measures.
Perform and document Impact Assessments and Corrective Actions for Equipment
Remediation s associated with out of tolerance calibration results.
Proactively identify and address safety related issues through Near Miss Reporting Process.
Review product designs with R&D, Sustaining, and AME engineers for optimized manufactur
ability and ease of assembly, from raw material to finish products.
Leverage Subject Matter Experts during problem solving exercise. Provide multiple what-if scenarios to find the best total cost solution with financial impacts and emphasis on delivery timelines.
Uses existing tools and best practices to report and track product and process metrics.
Informs others proactively about developments or issues that affect their work, and their ability to meet commitments.
What You'll Bring
Bachelor s Degree in Engineering.
0-2+ years of experience
Preferred:
Experience in the Medical Device or a similar regulated industry. Knowledge or experience in SAP, CAD modeling,
schematic drafting, and electrical design knowledgeedge is a plus. Knowledge or experience in computer based automated testing.
This is where your expertise helps people!
You are a problem solver.
Complex projects or unexpected challenges are just opportunities to bring your considerable
abilities to use.
Whether working independently or with a trusted team, you are always ready to tackle a project and work hard to find solutions.
Your talent is needed across a wide variety of industries.
As a Manufacturing Engineer you have a wide array of career choices, but are motivated by the opportunity to work in a company that supports innovation, professional development, and a purposeful mission.
Your Team
We are a team of inquisitive individuals who embrace a collaborative environment to take on sophisticated challenges that meet the needs of our patients.
We often need to change directions and respond to issues to avoid disruptions in our fast-paced manufacturing environment.
Together, we build and maintain a positive work environment. Our team is dedicated to quality.
Delivering life-saving products is about getting them right, and our technical expertise
and experience working in a manufacturing environment empower us to meet that challenge.
When you join us, you will work with a team of committed individuals who trust each other to deliver on the tasks at hand.
We support innovation and out-of-the-box thinking balanced with collaboration across functions and other teams.
Our leadership understands the need for continuous education and provides opportunities for further development.
What You'll Be Doing
Member of cross functional Electronics Gemba Team with responsibility for up to 8
medical device manufacturing assembly lines.
Execute Process and Equipment Validation/Verification Strategies for new or changing manufacturing process elements.
Represent manufacturing on R&D project core teams, responsible for deliverables, collaborating with internal stakeholders and ensuring productivity.
Develop and maintain manufacturing process documentation including but not limited to:
Manufacturing Process Speci fications, Device History Records, Tooling/Equipment Specifications, Preventative Maintenance and Calibration procedures through Engineering
Change Management (ECM) process.
Perform and document root-cause analysis for
Non-Conforming Material Reports.
Summarize and report on departmental Safety, Quality, Delivery, Productivity, and Cost performance measures.
Use Lean/Six Sigma methodology to identify
and drive Continuous Improvement Projects to enhance Safety, Quality, Delivery, Productivity, and Cost performance measures.
Perform and document Impact Assessments and Corrective Actions for Equipment
Remediation s associated with out of tolerance calibration results.
Proactively identify and address safety related issues through Near Miss Reporting Process.
Review product designs with R&D, Sustaining, and AME engineers for optimized manufactur
ability and ease of assembly, from raw material to finish products.
Leverage Subject Matter Experts during problem solving exercise. Provide multiple what-if scenarios to find the best total cost solution with financial impacts and emphasis on delivery timelines.
Uses existing tools and best practices to report and track product and process metrics.
Informs others proactively about developments or issues that affect their work, and their ability to meet commitments.
What You'll Bring
Bachelor s Degree in Engineering.
0-2+ years of experience
Preferred:
Experience in the Medical Device or a similar regulated industry. Knowledge or experience in SAP, CAD modeling,
schematic drafting, and electrical design knowledgeedge is a plus. Knowledge or experience in computer based automated testing.
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