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Manufacturing Engineer I Location:
Temecula CA (100% Onsite)
Duration:
1+ Month
Shift Time:
5:00am to 1:30pm
Pay Range:
$38/hr to $41/hr (On W2)
We are looking for a “Manufacturing Engineer” to join one of our Fortune 500 clients.
Job Summary The Associate Manufacturing Engineer will serve as the primary manufacturing engineer supporting operations in Vascular Temecula. The individual will integrate with the team supporting the manufacturing line including the line supervisor, Quality Engineer, and operators to address opportunities found in their assigned line. They will be accountable for quality, safety, product output, and yield for their assigned manufacturing line and may also have a contributing role as a sustaining engineer for the department.
Job Responsibilities
Daily support of manufacturing activities to meet goals for safety, quality, cost, and production.
Maintain systems that support monitoring of key performance indicators such as yield, nonconforming material, or lead time and plan and implement changes when there is an adverse trend.
Work with line support team to perform line situation triage and determine non-conformance and initial containment.
Prepare product and process reports by collecting, analyzing, and summarizing information and trends.
Product/process knowledge and understanding of basic cause and effect of line and process changes.
Understand potential risk related to product nonconformance and have knowledge and expertise on product requirements and specifications.
Stay current and keep aware of the changing technical and competitive environment as it relates to the business.
Establish a means of keeping abreast with technology in own engineering area and share with co‑workers.
Ensure production line output meets product specifications.
Clear criteria of conforming/non-conforming product and online reliability test methods used for verifying conformance.
Maintain manufacturing documentation such as process instructions, lot history records, bill of materials.
Investigate, conduct test or experiments, gather data, perform preliminary analysis, and report findings.
Prepare and communicate recommendations and action plans.
Lead root cause analysis efforts for basic manufacturing events using DMAIC and A3s and support CAPA investigations.
Line support representative for yield improvements, cost improvement projects, productivity, quality and safety.
Responsible for simple continuous improvement projects development and execution.
Evaluate ideas from the Localized Process Improvement program for potential implementation.
Review existing layouts and standards and create a proposed design.
Perform validation activities for new or existing production lines, meeting regulatory requirements.
Support maintenance technicians and supervisors in equipment availability issues.
Review equipment work order completion and perform product impact analysis to release equipment for commercial use.
Assist in training personnel required for equipment operation.
Work with QA counterpart to determine quality impact of out-of-tolerance situations.
Execute line-related change management and change orders related to manufacturing line changes.
Comply with all regulations and standards for Quality, Environment, Health, Safety and Energy (EHS&E) Global Policies and Engineering Standards.
Education
Bachelor’s Degree
Minimum 1 year experience or up to 3 years of experience overall and any industry-specific experience needed.
Knowledge and proficiency in application and principles of Manufacturing & Process Engineering.
Effective cross‑functional communication to assist in resolving Quality/Engineering issues.
Knowledge of common office applications: Word, PowerPoint, Excel.
Basic understanding of materials, product design, product testing.
Preferred Experience
Basic understanding and knowledge of statistics, GD&T, tolerance stack up analysis, SPC, DOE fundamentals, and problem‑solving methodologies.
Familiar with inspection tools such as pin gauge, caliper, micrometer, snap gauge, drop gauge, block gauge, optical comparator, vision system, etc.
Experience in a medical device manufacturing environment such as extrusion, injection molding, laser cutting, cleaning, passivation, electropolishing, assembly, bonding, packaging, testing, inspection methods, and others.
Experience with statistical software, Six Sigma training or certification, SolidWorks or similar CAD, MS Project, Verification & Validation activities, basic understanding of FDA, GMP and ISO guidelines.
Ability to travel approximately 5%, including internationally.
We are looking for the candidate who are eligible to work with any employer without sponsorship.
If you’re interested, please click “Apply” button.
#J-18808-Ljbffr
Manufacturing Engineer I Location:
Temecula CA (100% Onsite)
Duration:
1+ Month
Shift Time:
5:00am to 1:30pm
Pay Range:
$38/hr to $41/hr (On W2)
We are looking for a “Manufacturing Engineer” to join one of our Fortune 500 clients.
Job Summary The Associate Manufacturing Engineer will serve as the primary manufacturing engineer supporting operations in Vascular Temecula. The individual will integrate with the team supporting the manufacturing line including the line supervisor, Quality Engineer, and operators to address opportunities found in their assigned line. They will be accountable for quality, safety, product output, and yield for their assigned manufacturing line and may also have a contributing role as a sustaining engineer for the department.
Job Responsibilities
Daily support of manufacturing activities to meet goals for safety, quality, cost, and production.
Maintain systems that support monitoring of key performance indicators such as yield, nonconforming material, or lead time and plan and implement changes when there is an adverse trend.
Work with line support team to perform line situation triage and determine non-conformance and initial containment.
Prepare product and process reports by collecting, analyzing, and summarizing information and trends.
Product/process knowledge and understanding of basic cause and effect of line and process changes.
Understand potential risk related to product nonconformance and have knowledge and expertise on product requirements and specifications.
Stay current and keep aware of the changing technical and competitive environment as it relates to the business.
Establish a means of keeping abreast with technology in own engineering area and share with co‑workers.
Ensure production line output meets product specifications.
Clear criteria of conforming/non-conforming product and online reliability test methods used for verifying conformance.
Maintain manufacturing documentation such as process instructions, lot history records, bill of materials.
Investigate, conduct test or experiments, gather data, perform preliminary analysis, and report findings.
Prepare and communicate recommendations and action plans.
Lead root cause analysis efforts for basic manufacturing events using DMAIC and A3s and support CAPA investigations.
Line support representative for yield improvements, cost improvement projects, productivity, quality and safety.
Responsible for simple continuous improvement projects development and execution.
Evaluate ideas from the Localized Process Improvement program for potential implementation.
Review existing layouts and standards and create a proposed design.
Perform validation activities for new or existing production lines, meeting regulatory requirements.
Support maintenance technicians and supervisors in equipment availability issues.
Review equipment work order completion and perform product impact analysis to release equipment for commercial use.
Assist in training personnel required for equipment operation.
Work with QA counterpart to determine quality impact of out-of-tolerance situations.
Execute line-related change management and change orders related to manufacturing line changes.
Comply with all regulations and standards for Quality, Environment, Health, Safety and Energy (EHS&E) Global Policies and Engineering Standards.
Education
Bachelor’s Degree
Minimum 1 year experience or up to 3 years of experience overall and any industry-specific experience needed.
Knowledge and proficiency in application and principles of Manufacturing & Process Engineering.
Effective cross‑functional communication to assist in resolving Quality/Engineering issues.
Knowledge of common office applications: Word, PowerPoint, Excel.
Basic understanding of materials, product design, product testing.
Preferred Experience
Basic understanding and knowledge of statistics, GD&T, tolerance stack up analysis, SPC, DOE fundamentals, and problem‑solving methodologies.
Familiar with inspection tools such as pin gauge, caliper, micrometer, snap gauge, drop gauge, block gauge, optical comparator, vision system, etc.
Experience in a medical device manufacturing environment such as extrusion, injection molding, laser cutting, cleaning, passivation, electropolishing, assembly, bonding, packaging, testing, inspection methods, and others.
Experience with statistical software, Six Sigma training or certification, SolidWorks or similar CAD, MS Project, Verification & Validation activities, basic understanding of FDA, GMP and ISO guidelines.
Ability to travel approximately 5%, including internationally.
We are looking for the candidate who are eligible to work with any employer without sponsorship.
If you’re interested, please click “Apply” button.
#J-18808-Ljbffr