Johnson & Johnson

Senior Product Development Engineer Surgical Robotics - OTTAVA

Johnson & Johnson$109K — $174K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical or Electrical Engineering required; Master's preferred.
  • Minimum four years of relevant engineering experience.
  • Familiarity with Design for Manufacturing (DFM) principles and injection molding processes.
  • Proficient in 3D CAD software (SolidWorks or Creo) and GD&T per ASME Y14.5.
  • Experience in regulated medical device development processes and standards.

Responsibilities

  • Collaborate with teams to develop and stabilize manufacturing processes for new products.
  • Implement manufacturing solutions using DFM, DFA, and cost principles.
  • Conduct design analyses to ensure robust manufacturability.
  • Drive cost-effective technical solutions through simplification and optimization.
  • Support design reviews to assess feasibility and manufacturability.
  • Liaise between teams to integrate manufacturing feedback into product design.
  • Oversee engineering builds and manage project deliverables.

Benefits

  • Participation in the company’s retirement plan and 401(k) savings plan.
  • Generous vacation and sick leave policies.
  • Parental leave of up to 480 hours for new parents.
  • Flexible time off for personal and family care.
  • Volunteer leave to support community service.
  • Comprehensive health benefit coverage.
Full Job Description
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.

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
  • Experience designing, developing, and testing the manufacturing of electromechanical, fiber, or laser equipment and systems, including test and process development.
  • Experience in Cost Engineering: Demonstrated experience in leading cost engineering initiatives, along with a solid track record of managing complex design projects with a focus on financial performance and strategic cost reductions.
  • Knowledgeable about medical-specific assembly technologies, the supplier equipment base, and the capabilities of the suppliers.
  • Process Excellence Six Sigma knowledge or certification.
  • Test methods development (TMD) & Test methods validation (TMV) experience.
  • Experience with one or more of the following: laser welding, riveting, laser etching, soldering, pressing, joining, extrusion, over molding, coating, and/or design for assembly experiences.

Other:
  • May require up to 30% of domestic and/or international travel to other sites and locations
  • The attendance policy required for this role is fully onsite.


#OTTAVASU

Required Skills:

Preferred Skills:
Business Requirements Analysis, Coaching, Corrective and Preventive Action (CAPA), Critical Thinking, Design Thinking, Feasibility Studies, Financial Competence, Health, Safety, and Environmental (HSE) Management, Lean Supply Chain Management, Mechanical Engineering, Problem Solving, Process Oriented, Product Design, Product Development, Project Management Methodology (PMM), Science, Technology, Engineering, and Math (STEM) Application, Technical Credibility, Technologically Savvy

The anticipated base pay range for this position is :
$109,000.00 - $174,800.00

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

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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