Associate Clinical Designer, Orthopedics

Biopharma Careers; Chester (Delaware County); In loco; USD 50.000 - 65.000; Tempo pieno

Descrizione del lavoro

Johnson & Johnson seeks an Associate Clinical Designer in West Chester, PA, for entry-level CAD design of mechanical medical devices. You will draft, design, and document patient-specific implants and surgical plans while coordinating with surgeons and cross-functional teams to ensure on-time delivery.

The role emphasizes collaboration with clinical coordinators, designers, and manufacturing partners, requiring strong problem solving, organizational, and leadership capabilities, with a focus on

Competenze

• Entry level position.
• Experience in the CAD design of mechanical products, including multi-component systems, preferably of customized medical devices is preferred.
• Associates degree in Mechanical Engineering or Engineering Drafting and Design (or equivalent professional experience) is preferred.

Mansioni

• Draft, design, develop and document patient specific implants, surgical plans, instruments and other projects.
• Work with marketing, product development engineers, surgeons, manufacturing and other team members to develop product requirements and concepts.
• Interact directly with medical professionals to understand and develop customized surgical plans and product designs.
• Provide feedback and input on next-generation customized product line programs and processes.
• Perform other special projects and functions as assigned.

Conoscenze

Organizational skills

Problem solving

Root cause analysis

Project leadership

Interpersonal skills

Formazione

Associates degree in Mechanical Engineering or Engineering Drafting and Design

Strumenti

MS Office Suite

Descrizione del lavoro

Johnson & JohnsonPosted October 20, 2026# Associate Clinical Designer, OrthopedicsWest Chester, United States Full timeClinical Development AssociateNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityAt 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 Operations**Job Sub Function:**Clinical/Medical Operations**Job Category:**Business Enablement/Support**All Job Posting Locations:**West Chester, Pennsylvania, United States of America**Job Description:****About MedTech**Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.Your unique talents will help patients on their journey to wellness. Learn more at **https://www.jnj.com/medtech**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. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.We are searching for the best talent for **Associate Clinical Designer** position.Responsible for the drafting, design, development and documentation of patient specific implants, surgical plans, instruments and other projects.Works closely with clinical coordinators, other clinical designers, surgeons, sales consultants and marketing staff. Responsible for managing multiple projects and ensure on-time completion of designs. Gathers and implements process improvement feedback to drive continuous improvement of the team. Competence in 1-2 TruMatch customized product lines.**You will be responsible for:**Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:**JOB SUMMARY**Responsible for the drafting, design, development and documentation of patient specific implants, surgical plans, instruments and other projects. Works closely with clinical coordinators, other clinical designers, surgeons, sales consultants and marketing staff. Responsible for managing multiple projects and ensure on-time completion of designs. Gathers and implements process improvement feedback to drive continuous improvement of the team. Competence in 1-2 TruMatch customized product lines.**DUTIES & RESPONSIBILITIES**Under general direction and in accordance with all applicable federal, state, and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, key responsibilities for this position include:Work with Marketing, Product Development Engineers, surgeons, manufacturing and other team members to develop product requirements and concepts.Interact directly with medical professionals to understand and develop customized surgical plans and product designs.Exhibit capability in at least 1 Trumatch customized product linesProvide feedback and input on next-generation customized product line programs and processesPerforms other special projects and functions as assigned.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.Responsible for communicating business related issues or opportunities to next management levelResponsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicableResponsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and proceduresPerforms other duties assigned as needed**EXPERIENCE AND EDUCATION**Entry level position. Experience in the CAD design of mechanical products, including multi-component systems, preferably of customized medical devices is preferred.Associates degree in Mechanical Engineering or Engineering Drafting and Design (or equivalent professional experience) is preferred.**REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS**Possess strong organizational skills to support all aspects of the customized product line and processExcellent problem solving, decision-making, and root cause analysis skills in addition to interpersonal skills that foster conflict resolution as it relates to technical situations is required.Must demonstrate a strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience.Demonstrated creative design ability.Proficiency utilizing the MS Office Suite (Word, Excel, PowerPoint, etc.) is required.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- Hybrid**Required Skills:****Preferred Skills:**Administrative Support, Analytical Reasoning, Business Behavior, Clinical Operations, Clinical Research and Regulations, Clinical Trial Designs, Communication, Data Analysis, Execution Focus, Innovation, Laboratory Operations, Preclinical Research, Process Oriented, Project Administration, Regulatory Compliance, Research and Development, Research Documents