Johnson & Johnson companies are equal opportunity employers.
SENIOR FRANCHISE OPERATIONS DEVELOPMENT ENGINEER-8095140102
Description
The Ethicon Surgical Care business combines products and services of two market leading legacy companies, both with long histories of medical innovation. Ethicon, Inc. based in Somerville, New Jersey, was founded more than 80 years ago as a pioneer in suture development and manufacturing, helping to transform the safety and electiveness of open surgery. Ethicon Endo-Surgery, Inc. was created 20 years ago in Cincinnati, Ohio, developing innovative devices that have driven the revolutionary shift from open to minimally invasive surgery that continues to lead the industry today.
Ethicon Endo Surgery Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Engineer in the Franchise Operations Development organization, supporting the Endo-Mechanical & Energy Development Engineering to be based in Cincinnati, OH.
Duties and Responsibilities:
Lead/support NPD project to plan, design, develop, qualify, validate and stabilize end to end assembly process solutions. Responsible for process characterization and control for component and assembly solutions. Provide input to NPD teams on Design for M, A , C and drive product development to enable robust product and process development that meets business commitments and stabilization metrics. Responsible for designing and developing robust equipment and processes to meet product requirements in compliance to Lean, Safety and Ergo requirements. Incorporates risk mitigation methodology to drive process stability and capability. Develop Verification and validation strategies for end-to end process validation. Develop methods and test solutions for product verification and validation testing. Develop robust process solutions for polymer and metallic components, ensuring on time product launches and with low cost as a focus. Plan, conduct & direct engineering assignments to completion. Lead improvements to product quality and production processes on LCM projects. Development, qualification, validation and stabilization of plastic, metal components. Apply comprehensive & diverse knowledge of engineering principles to a broad range of assignments. Write and review documentation related to procedures, special instructions, qualification plans and reports, corrective action plans, etc. Deliver departmental goals and objectives for continuous improvement, Financial, and franchise initiatives. Ability to function and drive the team to execute in ambiguous situations, with a sense of urgency. Experience working with external suppliers to drive component and assembly process solutions. Pro-actively develop technology solutions to mitigate risk associated with NUD product requirements. Ability to identify and translate work content associated with process development required for NPD projects into resourcing needs. Support Project management activities of the Project leadership. Provide leadership and mentor less experienced engineering talent. Champion Systems development strategy and support operations strategy in end to end supply chain solution development. Responsible for the process development, verification and validation strategy and execution to the strategy.
J2W:LI
Qualifications
A minimum of a Bachelor's degree in Engineering is required, preferably in Mechanical, Material Science, Bio-Engineering, or Electrical Engineering discipline; Advanced Engineering degree is preferred.
A minimum of 5 years with Bachelors or at least 3 years and a Masters of combined engineering experience in a regulated industry is required; Prior experience in R&D/ New product development is preferred
Previous experience in the area of Design for Manufacturing & Assembly (DFM & A) is required.
Experience within a medical device production environment or other health care regulated environment preferred
Demonstrated success in leading individuals and coordinating team activities in a matrix environment is preferred.
Prior project management experience required, PMP certification is desirable
Experience in equipment and assembly process development in CFM (Continuous Flow Manufacturing) environment is preferred.
Experience in the development and implementation of automated assembly systems along with experience with PLC, HMI and Vision controls preferred
Experience with metal component design, development, and production processes is preferred.
Experience with plastic component design, development, and production processes is preferred.
Experience in design, development, implementation and stabilization of Measurement Systems preferred.
A strong background in advanced Statistical Process Control (SPC) is required.
Experience with mechanical and/or electro mechanical component development is required.
Knowledge of GD&T (ASME Y14.5, 1994) is required for application in NPD projects
Assembly process development is required.
Six Sigma / Process Excellence and/or Design Excellence experience is preferred. A Six Sigma / Design Excellence Certification is preferred.
Experience in Electro-Mechanical systems is preferred
Experience in CAD software (NX or Solid works) usage is preferred
Must be able to travel approximately 20% domestic and internationally (including Juarez, Mexico).
Strong analytical and problem solving skills
Demonstrated ability for teamwork and collaboration, strong attention to detail and having a sense of urgency.
Ability to delegate, coordinate and direct engineering assignments to team members and be accountable for their deliverables
Understanding of SCOR model of Supply Chain is preferred
Excellent communication and interpersonal skills required.
Knowledge of FDA/ISO requirements associated with the development of medical devices including Design Control preferred
Understanding of IP issues relative to processes being developed preferred.
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 FRANCHISE OPERATIONS DEVELOPMENT ENGINEER-8095140102
Description
The Ethicon Surgical Care business combines products and services of two market leading legacy companies, both with long histories of medical innovation. Ethicon, Inc. based in Somerville, New Jersey, was founded more than 80 years ago as a pioneer in suture development and manufacturing, helping to transform the safety and electiveness of open surgery. Ethicon Endo-Surgery, Inc. was created 20 years ago in Cincinnati, Ohio, developing innovative devices that have driven the revolutionary shift from open to minimally invasive surgery that continues to lead the industry today.
Ethicon Endo Surgery Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Engineer in the Franchise Operations Development organization, supporting the Endo-Mechanical & Energy Development Engineering to be based in Cincinnati, OH.
Duties and Responsibilities:
Lead/support NPD project to plan, design, develop, qualify, validate and stabilize end to end assembly process solutions. Responsible for process characterization and control for component and assembly solutions. Provide input to NPD teams on Design for M, A , C and drive product development to enable robust product and process development that meets business commitments and stabilization metrics. Responsible for designing and developing robust equipment and processes to meet product requirements in compliance to Lean, Safety and Ergo requirements. Incorporates risk mitigation methodology to drive process stability and capability. Develop Verification and validation strategies for end-to end process validation. Develop methods and test solutions for product verification and validation testing. Develop robust process solutions for polymer and metallic components, ensuring on time product launches and with low cost as a focus. Plan, conduct & direct engineering assignments to completion. Lead improvements to product quality and production processes on LCM projects. Development, qualification, validation and stabilization of plastic, metal components. Apply comprehensive & diverse knowledge of engineering principles to a broad range of assignments. Write and review documentation related to procedures, special instructions, qualification plans and reports, corrective action plans, etc. Deliver departmental goals and objectives for continuous improvement, Financial, and franchise initiatives. Ability to function and drive the team to execute in ambiguous situations, with a sense of urgency. Experience working with external suppliers to drive component and assembly process solutions. Pro-actively develop technology solutions to mitigate risk associated with NUD product requirements. Ability to identify and translate work content associated with process development required for NPD projects into resourcing needs. Support Project management activities of the Project leadership. Provide leadership and mentor less experienced engineering talent. Champion Systems development strategy and support operations strategy in end to end supply chain solution development. Responsible for the process development, verification and validation strategy and execution to the strategy.
J2W:LI
Qualifications
A minimum of a Bachelor's degree in Engineering is required, preferably in Mechanical, Material Science, Bio-Engineering, or Electrical Engineering discipline; Advanced Engineering degree is preferred.
A minimum of 5 years with Bachelors or at least 3 years and a Masters of combined engineering experience in a regulated industry is required; Prior experience in R&D/ New product development is preferred
Previous experience in the area of Design for Manufacturing & Assembly (DFM & A) is required.
Experience within a medical device production environment or other health care regulated environment preferred
Demonstrated success in leading individuals and coordinating team activities in a matrix environment is preferred.
Prior project management experience required, PMP certification is desirable
Experience in equipment and assembly process development in CFM (Continuous Flow Manufacturing) environment is preferred.
Experience in the development and implementation of automated assembly systems along with experience with PLC, HMI and Vision controls preferred
Experience with metal component design, development, and production processes is preferred.
Experience with plastic component design, development, and production processes is preferred.
Experience in design, development, implementation and stabilization of Measurement Systems preferred.
A strong background in advanced Statistical Process Control (SPC) is required.
Experience with mechanical and/or electro mechanical component development is required.
Knowledge of GD&T (ASME Y14.5, 1994) is required for application in NPD projects
Assembly process development is required.
Six Sigma / Process Excellence and/or Design Excellence experience is preferred. A Six Sigma / Design Excellence Certification is preferred.
Experience in Electro-Mechanical systems is preferred
Experience in CAD software (NX or Solid works) usage is preferred
Must be able to travel approximately 20% domestic and internationally (including Juarez, Mexico).
Strong analytical and problem solving skills
Demonstrated ability for teamwork and collaboration, strong attention to detail and having a sense of urgency.
Ability to delegate, coordinate and direct engineering assignments to team members and be accountable for their deliverables
Understanding of SCOR model of Supply Chain is preferred
Excellent communication and interpersonal skills required.
Knowledge of FDA/ISO requirements associated with the development of medical devices including Design Control preferred
Understanding of IP issues relative to processes being developed preferred.
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