Senior Product Development Engineer Surgical Robotics – OTTAVA

Johnson & Johnson Co.; Santa Clara (CA); Sur place; USD 120 000 - 170 000; Plein temps

Résumé du poste

Johnson & Johnson RAD (Robotics and Digital) in Santa Clara is seeking a Senior Product Development Engineer Surgical Robotics – OTTAVA to drive New Product Development and introduction for surgical robotics solutions. Lead cross-functional teams, manage design decisions, and ensure regulatory compliance across the development lifecycle.

You will collaborate with R&D, Manufacturing, and Suppliers to deliver robust, manufacturable designs that meet 21 CFR 820, ISO 13485 standards and ISO 14971

Qualifications

• Bachelor's degree in Mechanical or Electrical Engineering; Master's preferred.
• Minimum four years of relevant professional experience.
• Experience in Design for Manufacturing or Assembly (DFM/A).
• Experience with regulated medical device development (21 CFR 820, ISO 13485, ISO 14971, IEC 60601).
• Proficiency in 3D CAD and GD&T.
• Experience working with external suppliers.
• Knowledge of MSA, DOE, PFMEA.

Responsabilités

• Develop robust component and manufacturing processes for NPD projects.
• Lead design reviews, risk assessments and design for manufacturability decisions.
• Collaborate with R&D, Manufacturing and suppliers to implement robust manufacturing solutions.
• Ensure designs meet GMP requirements and regulatory guidelines.

Connaissances

Problem solving

Cross-functional collaboration

Technical communication

Formation

Bachelor’s degree in Mechanical or Electrical Engineering

Master’s degree preferred

Outils

3D CAD (SolidWorks/Creo)

GD&T (ASME Y14.5)

DOE

PFMEA

GR&R

Description du poste

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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:

Supply Chain Engineering

Job Sub Function:

Mechanical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

Johnson & Johnson RAD (Robotics and Digital) is seeking for a Senior Product Development Engineer Surgical Robotics – OTTAVA , for our Santa Clara, Location.

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 athttps://www.jnj.com/ (https://www.jnj.com/.

About MedTechSurgery

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

Are you passionate about improving and expanding the possibilities of surgery? Ready to join a teamthat’sreimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovasculardiseaseand cancer. Patients are waiting.

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

Purpose:

Our team of engineers, designers, and technical specialists is at the forefront of innovation in the medical device industry. As a Senior Product Development Engineer , you will play a critical role in the New Product Development (NPD) and New Product Introduction (NPI) pipeline—driving solutions that translate cutting‑edge technology into meaningful improvements in patient care. The Development Engineering team works closely with cross‑functional partners and suppliers to deliver robust component designs and manufacturable processes that meet or exceed all product and regulatory requirements.

In this role, you will serve as a key technical contributor, collaborating with multidisciplinary engineering teams to develop complex, highly regulated medical devices. Senior‑level expectations include taking ownership of design elements, leading technical problem‑solving efforts, and influencing design decisions across functions. You are expected to apply advanced electrical and mechanical engineering expertise, independently resolve complex technical challenges, and proactively identify risks and opportunities throughout the development lifecycle. Strong communication skills are essential, as this role requires effective collaboration across engineering teams, suppliers, and associated management to drive alignment and execution in a fast‑paced, dynamic environment.

Key Responsibilities:

• Collaborate with internal teams and external suppliers to plan, develop, qualify, and stabilize component, equipment, and manufacturing processes for NPD projects.
• Partner with R&D, Manufacturing, and Suppliers to implement robust manufacturing solutions using DFM, DFA, and Design‑to‑Cost principles.
• Conduct tolerance stack‑up, GD&T and FEA analysis to ensure designs are robust and manufacturable at volume
• Drive cost‑effective technical solutions through design simplification, material optimization, and process improvements—without compromising quality or performance.
• Support formal design reviews by assessing technical feasibility, manufacturability, and cost trade‑offs to inform design decisions early.
• Serve as the liaison between R&D, Product Management, Quality, Manufacturing and suppliers, ensuring the voice of manufacturing is embedded in product design.
• Support Design Transfer activities to enable a smooth and compliant transition into manufacturing.
• Apply engineering fundamentals, advanced manufacturing techniques, and statistical analysis to solve complex technical problems and establish new methods and standards.
• Lead or support PFMEAs, process characterization, and control strategies in compliance with GMP requirements.
• Oversee engineering builds and pilot runs, performing root cause analysis and driving corrective actions.
• Manage project deliverables and track component and design changes to minimize impact to assembly and manufacturing operations.

Qualifications:

Education: A minimum of a Bachelor’s degree and/or equivalent University degree is required; a focused degree in Mechanical or Electrical Engineering field or a related field is preferred. An advanced degree, Master’s is preferred.

Required

• Minimum four (4) years of relevant professional work experience
• Engineering experience in either mechanical, electro‑mechanical, or opto‑mechanical and components or equipment.
• Experience in Design for Manufacturing or Assembly (DFM/A) around injection molding, machining, and optical equipment.
• Proficiency in 3D CAD (SolidWorks or Creo) and GD&T per ASME Y14.5
• Technical Knowledge: Strong understanding of cost implications on design requirements, alongside broad engineering knowledge in developing and implementing manufacturing processes that meet or exceed product requirements.
• Experience working closely with external or third‑party suppliers.
• Knowledge and demonstrated application of regulated medical device development processes, standards, and guidelines, including but not limited to 21 CFR 820, ISO 13485, ISO 14971, and IEC 60601.
• Measurement Systems Analysis experience (e.g., GR&R).
• Statistical Analysis knowledge (e.g., Design of Experiments (DOE), Process Stability/Control/Capability) and PFMEA.
• Understand equipment concept creation, review approval, build, runoff, FAT, software validation, IQ, OQ, and PQ road map requirements.
• Proven interpersonal and communication skills, with the ability to work successfully in a team environment.
• Strong technical communication skills and proven ability to work independently.

Preferred:

• Understanding of regulatory requirements regarding the design, build, and release of medical devices, worldwide