Johnson & Johnson companies are equal opportunity employers.
SENIOR DESIGN ENGINEER - ANALYTICS-2289131009
Description
Ethicon Endo- Surgery, Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for a R&D Senior Product Design Engineer, located in Cincinnati, OH.
ETHICON Energy is a leader in the dynamic high growth advanced energy marketplace and is positioned for sustained double digit growth with its broad portfolio of innovative products and a deep pipeline of advanced technologies. Our diverse suite of ultrasonic and advanced bipolar energy devices are used to cut and seal tissue and vessels in open and laparoscopic surgical procedures. ETHICON’s portfolio consists of market leading HARMONIC® ultrasonic devices that empower surgeons to handle multiple jobs with superior precision and the rapidly growing ENSEAL® advanced bipolar devices that assure superior tissue sealing. These devices enable customers to achieve superior outcomes with solutions that deliver strong clinical & economic value propositions, superior tissue effects and intuitive use. The versatility and effectiveness of these devices enables them to be used in a wide range of minimally invasive surgical procedures including: Bariatric, Colorectal, General, Gynecologic, Head and Neck, Plastic, Thoracic, Orthopedic and Urology.
Our R&D team of engineers, designers and technical experts are in the forefront of technology in the medical device industry. You will be making a vital contribution to the New Product Development pipeline and transforming patient care through innovation. Our Design Engineer executes specific & general assignments/projects that provide innovative, functional, cost effective & validated product designs in a team based environment.
KEY JOB RESPONSIBILITIES:
Apply knowledge of general engineering principles, materials, DFMA & reliability to achieve product design requirements.
Work one-on-one with customer stakeholders to identify procedure and/or product opportunities and evaluate potential technical solutions. Interpret customer & marketing input to define technical design requirements. Maintain idea notebooks. Utilize QFD (quality function & deployment) JOC (jobs, outcomes & constraints), VOC (voice of customer) methodologies & surgical procedure knowledge to define product & design options. Provide innovative product, system & component design solutions. Perform detailed design analysis & provide input or approval for detailed design specifications. Establish appropriate testing strategy to insure adequate safety factors or margins. Perform product testing
to insure adequate safety factors or margins. Formalize concepts, breadboards & prototyping. Provide support to patent attorneys for patent filing. Consult with materials technology group for biomaterial approvals. Assist in developing & monitoring project plan, budget, contingency plans & work estimation. Coordinate integration of complex sub-system product designs. Provide technical leadership to product development team. Learn medical terminology, procedures & instrumentation. Provide peer feedback & may mentor junior associates as required.
TECHNICAL (MECHANICAL)
Develop free-body diagrams, calculate stress & strain values, and formulate tolerance stack-ups.
Develop error budget analyses of electromagnetic & electromechanical systems
Other responsibilities may be assigned & not all responsibilities listed may be assigned
Qualifications
BS or MS engineering degree (preferably Mechanical Engineering), with 5 + years of design-related experience required (preferably in medical products or device industry working in a team base environment). Knowledge of general design engineering and DFMA principles, component manufacturing processes, tooling methodologies, material properties, and regulatory compliance required. Experience with CAD/CAM and design analysis software, and Statistical analysis techniques is required. This role will also requires demonstrated technical leadership capabilities with experience working in a cross-functional team environment. Experience working with Vendors and Suppliers is required . Basic knowledge & understanding of medical regulatory requirements is a asset for this role. Technical writing is required with protocols, testing results, procedures, status & special reports as preferred. Project management skills are an asset. Knowledge & understanding of medical regulations & their impact on business, ISO (International Organization for Standardization) & GMP (Good Manufacturing Practices). Information & risk analysis skills are preferred. Quality, statistical process controls are assets. Knowledge of part manufacturing processes & tooling methodologies are assets. Effective team interpersonal skills. Conflict analysis & resolution. Consulting, design review, & constructive feedback Negotiating (e.g., internal & external customers), Networking, Able to adapt to shifting priorities, Able to handle rapid pace environment. Able to resolve problems / conflicts, Able to take initiative & be self-managing. General design engineering principles, Design of experiments (DOE), DFMA (design for manufacturing and assembly) principles, Patent interpretation, Mechanical testing): Free-body & stress-strain analysis is required & FEA (finite element analysis) ,Geometric tolerance & tolerance stack-up analysis (GD&T). Gage repeatability & re-calibration system & methodology, Plastic resins, ferrous & nonferrous metals, adhesives & sealants. Expertise creating scientific applications including, object oriented programming and GUI development, utilizing Python, C++, and/or Java is an asset. Experience in customizing Simulia Abaqus through Python scripting in automated model creation and output database results extension is a preferred skill Experience creating user subroutines for use in Simulia Abaqus is a plus for this role. Experience with MATLAB is preferred for this position.
It will be required, in the position, to have experience in Structural Finite Element Analysis and the use of ABAQUS is an asset for this role.
If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI
Primary Location:North America-United States-Ohio-Cincinnati
Organization: Ethicon Endo Surgery Inc (6041)
Job Function: R&D Engineering (R&D)
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
SENIOR DESIGN ENGINEER - ANALYTICS-2289131009
Description
Ethicon Endo- Surgery, Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for a R&D Senior Product Design Engineer, located in Cincinnati, OH.
ETHICON Energy is a leader in the dynamic high growth advanced energy marketplace and is positioned for sustained double digit growth with its broad portfolio of innovative products and a deep pipeline of advanced technologies. Our diverse suite of ultrasonic and advanced bipolar energy devices are used to cut and seal tissue and vessels in open and laparoscopic surgical procedures. ETHICON’s portfolio consists of market leading HARMONIC® ultrasonic devices that empower surgeons to handle multiple jobs with superior precision and the rapidly growing ENSEAL® advanced bipolar devices that assure superior tissue sealing. These devices enable customers to achieve superior outcomes with solutions that deliver strong clinical & economic value propositions, superior tissue effects and intuitive use. The versatility and effectiveness of these devices enables them to be used in a wide range of minimally invasive surgical procedures including: Bariatric, Colorectal, General, Gynecologic, Head and Neck, Plastic, Thoracic, Orthopedic and Urology.
Our R&D team of engineers, designers and technical experts are in the forefront of technology in the medical device industry. You will be making a vital contribution to the New Product Development pipeline and transforming patient care through innovation. Our Design Engineer executes specific & general assignments/projects that provide innovative, functional, cost effective & validated product designs in a team based environment.
KEY JOB RESPONSIBILITIES:
Apply knowledge of general engineering principles, materials, DFMA & reliability to achieve product design requirements.
Work one-on-one with customer stakeholders to identify procedure and/or product opportunities and evaluate potential technical solutions. Interpret customer & marketing input to define technical design requirements. Maintain idea notebooks. Utilize QFD (quality function & deployment) JOC (jobs, outcomes & constraints), VOC (voice of customer) methodologies & surgical procedure knowledge to define product & design options. Provide innovative product, system & component design solutions. Perform detailed design analysis & provide input or approval for detailed design specifications. Establish appropriate testing strategy to insure adequate safety factors or margins. Perform product testing
to insure adequate safety factors or margins. Formalize concepts, breadboards & prototyping. Provide support to patent attorneys for patent filing. Consult with materials technology group for biomaterial approvals. Assist in developing & monitoring project plan, budget, contingency plans & work estimation. Coordinate integration of complex sub-system product designs. Provide technical leadership to product development team. Learn medical terminology, procedures & instrumentation. Provide peer feedback & may mentor junior associates as required.
TECHNICAL (MECHANICAL)
Develop free-body diagrams, calculate stress & strain values, and formulate tolerance stack-ups.
Develop error budget analyses of electromagnetic & electromechanical systems
Other responsibilities may be assigned & not all responsibilities listed may be assigned
Qualifications
BS or MS engineering degree (preferably Mechanical Engineering), with 5 + years of design-related experience required (preferably in medical products or device industry working in a team base environment). Knowledge of general design engineering and DFMA principles, component manufacturing processes, tooling methodologies, material properties, and regulatory compliance required. Experience with CAD/CAM and design analysis software, and Statistical analysis techniques is required. This role will also requires demonstrated technical leadership capabilities with experience working in a cross-functional team environment. Experience working with Vendors and Suppliers is required . Basic knowledge & understanding of medical regulatory requirements is a asset for this role. Technical writing is required with protocols, testing results, procedures, status & special reports as preferred. Project management skills are an asset. Knowledge & understanding of medical regulations & their impact on business, ISO (International Organization for Standardization) & GMP (Good Manufacturing Practices). Information & risk analysis skills are preferred. Quality, statistical process controls are assets. Knowledge of part manufacturing processes & tooling methodologies are assets. Effective team interpersonal skills. Conflict analysis & resolution. Consulting, design review, & constructive feedback Negotiating (e.g., internal & external customers), Networking, Able to adapt to shifting priorities, Able to handle rapid pace environment. Able to resolve problems / conflicts, Able to take initiative & be self-managing. General design engineering principles, Design of experiments (DOE), DFMA (design for manufacturing and assembly) principles, Patent interpretation, Mechanical testing): Free-body & stress-strain analysis is required & FEA (finite element analysis) ,Geometric tolerance & tolerance stack-up analysis (GD&T). Gage repeatability & re-calibration system & methodology, Plastic resins, ferrous & nonferrous metals, adhesives & sealants. Expertise creating scientific applications including, object oriented programming and GUI development, utilizing Python, C++, and/or Java is an asset. Experience in customizing Simulia Abaqus through Python scripting in automated model creation and output database results extension is a preferred skill Experience creating user subroutines for use in Simulia Abaqus is a plus for this role. Experience with MATLAB is preferred for this position.
It will be required, in the position, to have experience in Structural Finite Element Analysis and the use of ABAQUS is an asset for this role.
If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W:LI
Primary Location:North America-United States-Ohio-Cincinnati
Organization: Ethicon Endo Surgery Inc (6041)
Job Function: R&D Engineering (R&D)
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement