Johnson & Johnson

Associate Development Engineer

In short

This Associate Development Engineer role at Johnson & Johnson's Orthopedics R&D team in Zuchwil, Switzerland involves supporting the design, development and lifecycle of implants and surgical instrumentation. The job requires close collaboration with cross-functional partners (R&D, Quality, Manufacturing, Regulatory, Marketing) and clinicians, plus mechanical testing, Design Control documentation and compliance with MDR/FDA requirements. It suits an early-career mechanical engineer with a bachelor's degree and at least 6 months of relevant design experience, CAD knowledge, and willingness to work with cadaver specimens in an operating room setting; business-fluent English is required.

About Orthopedics
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 Orthopedics? Ready to join a team that's reimagining how we heal? Our Orthopedics 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 the best talent for an Associate Development Engineer role.
Purpose
Join our R&D team and contribute to the development of innovative medical devices, including implants and surgical instrumentation. Working within a cross-functional team, you will help translate clinical needs into effective engineering solutions while supporting products throughout their lifecycle.
You will be responsible for
•Support the design and development of new implants, surgical instrumentation and existing products.
•Collaborate with R&D, healthcare professionals, Quality, Manufacturing, Regulatory, Marketing and other cross-functional partners to define product and design requirements.
•Support the development of engineering concepts, drawings, prototypes and Design Control documentation.
•Contribute to mechanical testing, verification and validation activities.
•Support product development and documentation in compliance with MDR, FDA Design Controls and applicable quality requirements.
•Participate in clinician interactions to support product development, improvements and modifications.
•Support design and process changes, production transfers, cost-improvement initiatives and quality/compliance activities.
•Participate in complaint and field investigations supporting patient and customer safety.
Qualifications and Requirements
•Bachelor's degree in Engineering or a related field; Mechanical Engineering preferred.
•At least 6 months of experience in mechanical product design and development, including internship, co-op or academic research experience.
•Knowledge of CAD tools such as Creo/ProE, mechanical design, manufacturing processes and GD&T is preferred.
•Knowledge of medical device development, Design Controls, GMP, QSR and ISO requirements is an advantage.
•Knowledge of biomechanics, anatomy and/or biology is an advantage.
•Strong problem-solving, communication and organisational skills, with the ability to manage multiple priorities.
•Willingness to work with wet tissue/cadaver specimens and in an operating room environment is required.
•Business-fluent English is required; German is preferred for German-speaking sites.
Johnson & Johnson announced plans to separate its Orthopedics business to establish a standalone orthopedics 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.
Preferred Skills: Bioinformatics, Biological Engineering, Biological Sciences, Biostatistics, Data Reporting, Data Savvy, Design of Experiments (DOE), Detail-Oriented, Execution Focus, Feasibility Studies, Preclinical Research, Problem Solving, Process Oriented, Prototyping, Report Writing, Research and Development, Researching, SAP Product Lifecycle Management, Technologically Savvy

Stop applying.
Get referred.

$10 in free credits

In just 60 seconds, fully on autopilot — Eraldt's AI agents read your CV, map the roles you fit, find live vacancies and the people who can refer you, write personal emails, and get you referred.

This isn't an application: your CV doesn't go to the company, and we don't promise a referral for this exact role.

Discover who else lands interviews on autopilot