Staff Product Development Engineer, MedTech Instruments

Johnson & Johnson MedTech; Santa Clara (CA); On-site; USD 134,000 - 231,000; Full time

Benefits offered by this job

Annual bonus

Medical benefits

401(k) plan

On-site in Santa Clara

Job summary

Johnson & Johnson MedTech is recruiting for a Staff Product Development Engineer, Instruments & Accessories in Santa Clara, CA. You translate clinical needs into robust hardware designs and drive risk management within Design Control across Monarch Instruments and Accessories.

Responsibilities include leading hardware development, requirements management, risk assessments, and cross-functional collaboration to ensure safe, effective devices and regulatory compliance.

Qualifications

• Bachelor’s degree in a biomedical or mechanical discipline.
• 8+ years of product development in medical devices or regulated industries.
• Strong Design Control, risk management and verification experience.
• Experience translating user needs into testable requirements; Jama familiarity.

Responsibilities

• Lead hardware development from concept to commercialization with Design Control.
• Define requirements, verification plans, and risk controls for devices.
• Collaborate with R&D, Manufacturing, Quality, Regulatory and PM teams.
• Mentor teams on requirements development and risk management best practices.

Skills

Design Control

Requirements Management

Risk Management

Design Verification

Cross-functional Collaboration

Communication

Hardware development

Education

Biomedical Engineering

Mechanical Engineering

Tools

Jama

Metal Injection Molding

Precision Machining

Job description

Johnson & Johnson MedTech is recruiting for a Staff Product Development Engineer, Instruments & Accessories in Santa Clara, CA. You translate clinical needs into robust hardware designs and drive risk management within Design Control across Monarch Instruments and Accessories.

Responsibilities include leading hardware development, requirements management, risk assessments, and cross-functional collaboration to ensure safe, effective devices and regulatory compliance.