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Product Development Engineer – Cases & Trays

Johnson & Johnson Innovative Medicine · West Chester, PA

Posted November 9, 2026

Mid levelProcess developmentOn site
US$78k to 127k a yearApply

Quick facts

Education
Bachelor's, or equivalent experience
Skills mentioned
Validation, 510(k) / device, Biostatistics, Bioinformatics, Inventory management

Pulled from the ad below. The full ad has the details.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

R&D Product Development

Job Sub Function

Biomedical Engineering

Job Category

Scientific/Technology

All Job Posting Locations

West Chester, Pennsylvania, United States of America

Job Description

About Orthopaedics

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for Product Development Engineer to be based out of West Chester, PA Or Zuchwil, Switzerland.

Purpose

Product Development Engineer – Cases & Trays is responsible for supporting the design, development, verification, and commercialization of surgical case and tray solutions for new product development and lifecycle programs.

The engineer works closely with Product Development, Design Engineering, Quality, Regulatory, Supply Chain, Manufacturing, Marketing, and external suppliers to translate product and user requirements into robust, manufacturable Cases & Trays solutions.

The role supports projects throughout the product development lifecycle, from early concept and product configuration through detailed development, verification, supplier qualification, design transfer, and product launch.

Key Responsibilities

Cases & Trays Product Development

  • Support the development of surgical cases, trays, caddies, brackets, inserts, and related components for implant and instrument systems.
  • Translate product, clinical, reprocessing, manufacturing, and user requirements into practical Cases & Trays solutions.
  • Develop case and tray concepts and configurations considering product grouping, capacity, instrument positioning, retention, stacking, handling, cleaning, and sterilization requirements.
  • Partner closely with Design Engineering resources to develop layouts, concepts, CAD models, drawings, prototypes, and production-ready designs.
  • Support design evaluations and recommend solutions that balance product protection, usability, reprocessing, manufacturability, cost, weight, and system complexity.
  • Leverage existing designs, standardized architectures, and lessons learned where appropriate to reduce development time, complexity, and unnecessary new SKUs.

Product Development & Project Execution

  • Execute assigned engineering activities throughout the product development lifecycle.
  • Develop and maintain engineering deliverables, schedules, technical documentation, and project actions.
  • Identify technical risks, issues, and dependencies and communicate them to the appropriate project stakeholders.
  • Participate in technical and design reviews and drive assigned actions to completion.
  • Coordinate engineering activities across Product Development, Design Engineering, Quality, Supply Chain, Manufacturing, and external suppliers.
  • Support prototype development, testing, design iterations, and technical assessments.
  • Communicate project status, technical issues, and recommendations clearly to project and functional stakeholders.
  • Manage multiple engineering priorities while maintaining quality and project commitments.

Supplier & Manufacturing Collaboration

  • Work directly with external Cases & Trays suppliers throughout product development.
  • Communicate technical requirements, design intent, quality expectations, and project deliverables.
  • Support supplier technical assessments, design reviews, prototype builds, manufacturability reviews, quotation activities, and qualification.
  • Collaborate with suppliers and internal partners to identify opportunities to improve manufacturability, assembly, quality, lead time, and cost.
  • Support investigation and resolution of supplier-related technical issues and nonconformances.
  • Support the successful transfer of designs into stable production.

Design Controls & Product Realization

  • Execute product development activities in accordance with applicable design controls, quality systems, and Product Realization processes.
  • Develop and maintain appropriate engineering documentation supporting design inputs, outputs, reviews, risk management, verification, validation, and design transfer.
  • Develop or support test protocols, engineering evaluations, reports, specifications, drawings, and other technical documentation.
  • Participate in product and process risk-management activities and support implementation of risk controls.
  • Support design verification and validation activities, including test planning, sample coordination, execution, data review, and report preparation.
  • Support engineering change activities throughout development and following product launch.
  • Maintain appropriate design traceability and ensure assigned technical documentation is completed accurately and on schedule.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Product Design Engineering , or a related engineering discipline.
  • Product development or engineering experience, preferably within medical devices, surgical instruments, orthopedics, or another regulated industry .
  • Experience applying engineering principles to the development of mechanical products or systems.
  • Understanding of engineering drawings, dimensional requirements, tolerances, and GD&T.
  • Experience with engineering testing, technical documentation, and structured problem solving.
  • Ability to work effectively with manufacturing partners and external suppliers.
  • Strong written, verbal, presentation, and cross-functional communication skills.
  • Ability to manage assigned engineering activities with appropriate guidance while actively driving issues to resolution.

Preferred Qualifications

  • Experience with surgical Cases & Trays, instruments, implants, sterilization containers, or reusable medical-device systems .
  • Knowledge of cleaning, sterilization, reprocessing, transportation, handling, and product-protection considerations for reusable surgical systems.
  • Experience with PCT Creo or equivalent 3D CAD software.
  • Experience with Windchill or another PLM system.
  • Working knowledge of GD&T and tolerance analysis.
  • Familiarity with design verification, validation, design transfer, and supplier qualification.
  • Experience working with external suppliers and geographically distributed engineering teams.
  • Familiarity with medical-device design controls and risk-management processes.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

#LI-PN2

Required Skills

Preferred Skills

AI Judgement Integration, Analytical Reasoning, Bioinformatics, Biological Engineering, Biological Sciences, Biostatistics, Coaching, Data Savvy, Detail-Oriented, Feasibility Studies, Inventory Management, Preclinical Research, Project Schedule, Prototyping, Research and Development, Researching, SAP Product Lifecycle Management, Technologically Savvy

The anticipated base pay range for this position is

$78,000.00 - $126,500.00

Additional Description for Pay Transparency

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company’s long-term incentive program.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits

Source: Johnson & Johnson Innovative Medicine's career site. PharmoniQ shows this job as posted and links to the original. Check the employer's page for the latest details.