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Engineer, Spine R&D

Job in Raynham, Bristol County, Massachusetts, 02767, USA
Listing for: Johnson & Johnson MedTech
Full Time position
Listed on 2026-07-08
Job specializations:
  • Engineering
    Product Engineer, Mechanical Engineer, Engineering Design & Technologists, Quality Engineering
Salary/Wage Range or Industry Benchmark: 76000 - 121900 USD Yearly USD 76000.00 121900.00 YEAR
Job Description & How to Apply Below

Company:
Johnson & Johnson – DePuy Synthes Orthopaedics

Job Function

R&D Product Development

Job Sub Function

Biomedical Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Raynham, Massachusetts, United States of America

Job Description

We are searching for the best talent to join our DePuy Synthes Orthopaedics team as an Engineer, Spine R&D based in Raynham, MA. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Our Orthopedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.

You

Will
  • Design and develop new products with high level direction from senior engineers/technical leads
  • Assist the project leader or DRI (Directly Responsible Individual) with planning and executing projects or portions of a project working closely with the PCT
  • Develop parametric CAD models and detailed drawings to support concept development and final designs per drawing/drafting standards
  • Develop layouts and tolerance studies utilizing GD&T and CAD assisted methods
  • Development and execution of engineering documentation related to assigned projects, such as technical reports, design verification and validation activities and assist in process validation.
  • Modify engineering drawings from new manufacturing methods or vendor specifications for design improvements in an effort to optimize designs for manufacturability and reduce COGS
  • Participate in preproduction meetings for new products.
  • Solve design related problems of existing products.
  • Develop clinical acumen for various spinal pathologies and procedures
  • Hands‑on testing of product in development in a cadaveric model
  • Uses analytical techniques and finite element analysis to assist product testing.
  • Conducts various hands‑on testing for design verification and test method developments.
  • Provide technical product support for surgeons and salesforce.
  • Demonstrate an ability to prioritize tasks and manage a varied workload, exhibit strong written and verbal communication skills and interface effectively with project teams.
  • Responsible for communicating business related issues or opportunities to next management level.
  • Performs other duties assigned as needed.
  • Support regulatory process for global registration efforts
Qualifications

Required:

  • Bachelor’s degree in Engineering
  • 2-4 years of relevant engineering experience.
  • Demonstrated ability to perform concept generation, technical feasibility and design engineering techniques.
  • In depth knowledge of manufacturing processes (i.e. milling, turning, EDM, etc.) and their limitations when designing products.
  • Experience creating or modifying computer‑generated 2D/3D CAD models and engineering drawings in alignment with company standards, including basic familiarity with GD&T and weld specifications.
  • Ability to effectively contribute to cross‑functional, multi‑disciplinary project teams.
  • Ability to manage multiple tasks simultaneously in a dynamic environment.
  • Understanding of concept generation, technical feasibility, and fundamental design engineering techniques, including familiarity with prototyping methods.
  • Ability to identify, communicate, and help resolve basic technical problems in a timely manner.
  • Basic understanding of time management principles and the ability to meet defined goals and commitments.
  • Ability to document work clearly and accurately, including adherence to good lab notebook practices and protection of confidential information.

Preferred:

  • Experience working in a regulated industry, preferably medical device manufacturing/design.
  • Understanding of design controls conforming to ISO 13485 and risk analysis conforming to ISO 14971.
  • Demonstrated ability to apply DFM and DFI principles and experience working with vendors to implement these principles into designs.
  • Familiarity with Design Excellence methodologies including DMADV.
  • Experience with mechanical experimental design including familiarity with test method validation.
  • Basic knowledge of materials used in surgical instruments or biomaterials, including ability to articulate selection…
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