Johnson & Johnson Careers

Associate Clinical Designer

West Chester, Pennsylvania
R&D Engineering (R&D)


Job Description

Requisition ID: 8493180410

DePuy Synthes Companies of Johnson & Johnson is seeking a Associate Clinical Designer  to be located in West Chester, PA.  

 

DePuy Synthes is a Johnson & Johnson company that is one of the leaders in the medical device industry.  Our implants and instruments are used by orthopaedic surgeons to treat patients with conditions resulting from traumatic injuries, degenerative diseases, deformities, and sports related injuries. Our environment is entrepreneurial, learning-driven, and is as challenging as it is rewarding.

 

DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Companies will 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, we are creating one organization that will be agile and better equipped in 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.


The Associate Clinical Designer be responsible for supporting the design and documentation of customized, patient-specific implants and instruments, based on a specific surgeon request and / or patient imaging.  For the design of patient-specific or surgeon-specific devices, this role includes checking all new requests and the corresponding imaging, importing and preparing the imaging and project data, preparing the project folder, and communicating with the sales consultants to ensure the specific requirements are understood and met.  This individual is responsible for supporting multiple cases, or implant designs, simultaneously, ensuring high quality, on-time completion of all design deliverables. 

 

The Associate Clinical Designer’s primary responsibilities will include:

 
  • Import, inspect and prepare patient imaging for future implant designs
  • Prepare the project folder, and register new cases in the project tracking software, and complete all updates in a timely manner
  • Request and inspect all functional check devices (FCD) for patient specific implants
  • Request anatomic models (if requested by the surgeon) from the supplier
  • Computer-aided design of less-complex patient-specific cranial devices, under the direct guidance of a Clinical Designer 2 or higher.
  • Interpret surgeon specifications and transfer the requirements into a patient-specific design that meets the surgeon’s needs and complies with the product requirements and indications.
  • Complete implant design reviews, ensuring compliance with all design standards and work instructions, including thorough and accurate design documentation based on the latest released procedures.
  • Ensure on-time execution of all project deliverables, including device designs, design reviews, quotations, and case correspondence.
  • Perform additional duties as assigned.
  • Understand and comply with all company policies in regards to HIPAA and patient confidentiality.
  • 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.


Qualifications
  • An Associates degree with a minimum of 2 years of relevant design experience OR a High School diploma with basic technical training in an Engineering/Drafting/Design field and a minium of 4 years relevant design experience is required.
  • Experience with 3D CAD software is required.
  • Experience with customized design processes is desirable.
  • Design for patient-specific devices is a plus.
  • Experience with MIMICS and FreeForm Modeler, ProENGINEER or Solidworks experience is a plus. CREO or WindChill is desired.
  • Experience working in manufacturing is a plus.
  • Experience working with 3D printing is a plus.
  • Demonstrated strong verbal and written communication skills.
  • Demonstrated high quality standards and a strong attention to details.
  • Demonstrated ability to prioritize, organize and manage multiple tasks.
  • Demonstrated the ability to effectively and efficiently learn and apply new technology.
  • This position will be based in West Chester, PA and may require up to 10% travel. 
 

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.


Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.




Primary Location
United States-Pennsylvania-West Chester
Organization
Synthes USA Products, LLC (6317)
Job Function
R&D Engineering (R&D)
Requisition ID
8493180410