Johnson & Johnson

Sr. NPI Engineer - Shockwave Medical

Johnson & Johnson$106K — $170K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical or Biomedical Engineering
  • Minimum 5 years experience in a medical device environment
  • Knowledge of FDA, ISO, and other Quality System regulations
  • Understanding of Lean and Six Sigma concepts
  • Experience with Validation of Medical Devices (IQ-OQ-PQ)
  • Able to create and maintain SolidWorks Drawings
  • Experience with ERP and MES systems (Oracle preferred)

Responsibilities

  • Collaborate with R&D, QA, RA, and Production on designing and implementing processes
  • Support Quality teams in addressing non-conformances
  • Analyze process performance for new product development
  • Identify and communicate process requirements to management
  • Maintain documentation for design control and quality requirements
  • Develop testing protocols for process verification and validation
  • Lead continuous improvement projects using DMAIC methodology

Benefits

  • Participation in retirement plans (pension and 401(k))
  • Eligibility for long-term incentive program
  • Vacation time of 120 hours per year
  • Sick time accrual up to 56 hours per year based on state of residence
  • Holiday pay including 13 days per year
  • Parental leave of up to 480 hours within a year of a child's arrival
  • Flexible caregiver and bereavement leave options
Full Job Description
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 Medical to join our team located in Santa Clara, CA.

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 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 requirements.
  • Employee may be required to lift objects up to 25lbs or more.
  • Employee will be required to work in an air-conditioned Class 8 Cleanroom.


Required Skills:

Preferred Skills:
Analytical Reasoning, Bioinformatics, Biological Engineering, Biological Sciences, Biostatistics, Coaching, Data Savvy, Detail-Oriented, Feasibility Studies, Inventory Management, Preclinical Research, Project Schedule, Prototyping, Research and Development, Researching, SAP Product Lifecycle Management, Technologically Savvy

The anticipated base pay range for this position is :
$106,000.00 - $170,200.00

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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