Product Development Engineer, Trauma (1of 2) Job
Company Name:
Depuy Orthopaedics. Inc. (6029)
West Chester, PA, US
Johnson & Johnson companies are equal opportunity employers.
Product Development Engineer, Trauma (1of 2
Description
DePuy Synthes Spine is currently recruiting for a Product Development Engineer, Trauma located in West Chester, PA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world.
DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today's evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.
Designs and develops new implants and instrumentation. This includes communication with
Surgeons and Sales Consultants, understanding the clinical issues, defining the design parameters to support AO philosophies, and ensuring the correct product is provided to the customer.
POSITION DUTIES &
Responsibilities:
Designs and develops new implants and instrumentation and develops improvements and modifications to current products; Interacts with surgeons, manufacturing, regulatory affairs, sales consultants, product managers, and other functional departments to define and develop product requirements and concepts; Works directly with surgeons for design concept development, prototype and cadaver evaluation, and clinical follow-up; Generates product models, concept layouts, and prints using a CAD software; Apply geometric dimensioning and tolerancing accordingly; Performs the required activities and generates the appropriate documents to ensure compliance with FDA Design Control regulations, and to support 510(k) submissions or IDE clinical studies; Develops mechanical test protocols according to ASTM standards and coordinates the activities required to fabricate test parts and complete mechanical testing; Works with manufacturing during the design stages to incorporate manufacturability into the product designs; Responsible for all the designs from concept development through product launch; Responsible for initial patent review of designs for freedom to operate; Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times; Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer; Performs other special projects and functions as assigned by the department manager.
Qualifications
A minimum of a Bachelor's degree in Mechanical Engineering Biomedical Engineering or another similar Engineering discipline is required. A minimum of 2 years work experience in product design / development or engineering is required. Mechanical design experience is required. Experience in design principles, material selection, ability to verify and validate design concepts, and understand design failure modes is required. Demonstrated understanding of various types of manufacturing, mechanisms, materials, proper tolerancing, drafting standards, and GD&T is an asset. Proficiency utilizing the MS Office Suite (Word, Excel, PowerPoint etc.) is required. Knowledge of CAD software (Pro Engineering, Pro-E, Solid Works, AutoCAD, etc.) is also an asset. Must have the ability to effectively communicate concepts, ideas and knowledge to other individuals, surgeons, customers and/or teams, and work effectively as a team member. Willing to work with cadavers and within an Operating Room setting is required. This position will be based in West Chester, PA and requires up to 30% travel, with a potential for international travel.
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 NA
Primary Location:
North America-United States-Pennsylvania-West Chester
Organization:
Depuy Orthopaedics. Inc. (6029)
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 SupplementEstimated Salary: $20 to $28 per hour based on qualifications.
Depuy Orthopaedics. Inc. (6029)
West Chester, PA, US
Johnson & Johnson companies are equal opportunity employers.
Product Development Engineer, Trauma (1of 2
Description
DePuy Synthes Spine is currently recruiting for a Product Development Engineer, Trauma located in West Chester, PA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world.
DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today's evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.
Designs and develops new implants and instrumentation. This includes communication with
Surgeons and Sales Consultants, understanding the clinical issues, defining the design parameters to support AO philosophies, and ensuring the correct product is provided to the customer.
POSITION DUTIES &
Responsibilities:
Designs and develops new implants and instrumentation and develops improvements and modifications to current products; Interacts with surgeons, manufacturing, regulatory affairs, sales consultants, product managers, and other functional departments to define and develop product requirements and concepts; Works directly with surgeons for design concept development, prototype and cadaver evaluation, and clinical follow-up; Generates product models, concept layouts, and prints using a CAD software; Apply geometric dimensioning and tolerancing accordingly; Performs the required activities and generates the appropriate documents to ensure compliance with FDA Design Control regulations, and to support 510(k) submissions or IDE clinical studies; Develops mechanical test protocols according to ASTM standards and coordinates the activities required to fabricate test parts and complete mechanical testing; Works with manufacturing during the design stages to incorporate manufacturability into the product designs; Responsible for all the designs from concept development through product launch; Responsible for initial patent review of designs for freedom to operate; Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times; Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer; Performs other special projects and functions as assigned by the department manager.
Qualifications
A minimum of a Bachelor's degree in Mechanical Engineering Biomedical Engineering or another similar Engineering discipline is required. A minimum of 2 years work experience in product design / development or engineering is required. Mechanical design experience is required. Experience in design principles, material selection, ability to verify and validate design concepts, and understand design failure modes is required. Demonstrated understanding of various types of manufacturing, mechanisms, materials, proper tolerancing, drafting standards, and GD&T is an asset. Proficiency utilizing the MS Office Suite (Word, Excel, PowerPoint etc.) is required. Knowledge of CAD software (Pro Engineering, Pro-E, Solid Works, AutoCAD, etc.) is also an asset. Must have the ability to effectively communicate concepts, ideas and knowledge to other individuals, surgeons, customers and/or teams, and work effectively as a team member. Willing to work with cadavers and within an Operating Room setting is required. This position will be based in West Chester, PA and requires up to 30% travel, with a potential for international travel.
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 NA
Primary Location:
North America-United States-Pennsylvania-West Chester
Organization:
Depuy Orthopaedics. Inc. (6029)
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 SupplementEstimated Salary: $20 to $28 per hour based on qualifications.
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