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Sr. NPI Engineer - Shockwave Medical

Johnson & Johnson MedTech · Santa Clara, CA

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Level
Senior
Team
Manufacturing
Base pay
$106k–$170k
Degree
Required
Experience asked
5+ years
Industry
Medical devices
Posted
30+ days ago

The role in 30 seconds

A senior manufacturing role at Johnson & Johnson MedTech (medical devices) in Santa Clara, CA.

They ask for
5+ years · degree required
Tools it names
Lean, Six Sigma, DMAIC, MSA / Gage R&R, DOE, FDA / GMP
Base pay
$106k–$170k

Read from the posting. The full description is below.

It asks for 5+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

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About the role

requirements

and consistent with FDA, ISO, MDR and other Quality System requirements.

  • ✓Prototype and develop designs, processes, and test methods in support of new product designs scaling for commercialization
  • ✓Develop protocols/reports and perform process verification and validation testing
  • ✓Represents Operations as a primary point of contact on manufacturing-related project activities, including internal and external requests and perform process-related tasks to support pilot manufacturing
  • ✓Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company’s product.
  • ✓Lead and/or actively participate in product/process engineering problem solving using DMAIC methodology.
  • ✓Lead and/or actively participate in process/product continuous improvement projects (in cooperation with development engineers and technicians).
  • ✓Apply Lean manufacturing principles in production processes to reduce/eliminate waste and increase productivity
  • ✓Assist Procurement and R&D departments with supplier selection and process development.
  • ✓Perform productivity and costing analyses (e.g., calculate direct labor & materials costs for new and existing products, identify and implement cost reduction plans for existing products).
  • ✓Other duties as assigned. These job

requirements

are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel.

Requirements

  • ✓Bachelor’s degree in Mechanical or Biomedical Engineering
  • ✓Min 5 years of experience in a medical device environment.
  • ✓Knowledge of and compliance with applicable Quality System

requirements

such as QSRs, FDA, ISO, MDD, MDR and other applicable regulations.

  • ✓Understanding of Lean and Six Sigma concepts.
  • ✓Experience with Validation of Medical Devices (IQ-OQ-PQ).
  • ✓Basic understanding of Statistics (Cpk, Hypothesis Testing, DOE’s, Gage R&R) a plus.
  • ✓Able to create and maintain Drawings in SolidWorks.
  • ✓Experience with ERP and MES (Oracle preferred)
  • ✓Knowledge of disposable peripheral and coronary device design, material selection, and testing preferred.
  • ✓Experience in early-stage catheter based cardiovascular devices project is a strong plus
  • ✓Effective communication skills with all levels of management and organizations
  • ✓Ability to work in a fast-paced environment while managing multiple priorities.
  • ✓Operate as a team and/or independently while demonstrating flexibility to changing requireme
Show full description ↓

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 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 Product Development

Job Sub Function

Biomedical Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Santa Clara, California, United States of America

Job Description

Johnson & Johnson is hiring for a Senior NPI Engineer – Shockwave Medica l to join our team located in Santa Clara, CA.

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 at https://www.jnj.com/.

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.

Position Overview

The NPI Senior Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production. The NPI Senior Engineer will work closely with production, quality, and R&D teams to support the company’s manufacturing operations and product launch timelines.

Essential Job Functions

  • •Work collaboratively with R&D, QA, RA and Production departments to design, develop, test, document and implement processes, tooling, and fixtures.
  • •Support and work with Quality to address and resolve non-conformances.
  • •Collect data and analyze process performance and capabilities for new processes development company products, including new products and products already in production.
  • •Identify process requirements, advise and support operations management, design and development implement equipment and fixturing needed for process development and manufacturing efforts.
  • •Develop and maintain documentation for design control, product configurations, manufacturing procedures, lot history records, (e.g., bills-of-materials, MPI’s, LHR’s), and company’s Design Control

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