Sr. Quality Engineer- Shockwave Medical

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

Job Function:

Supply Chain Engineering

Job Sub Function:

Quality Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Santa Clara California United States of America

Job Description:

Johnson & Johnson is hiring for aSr Quality Engineerfor Shockwave Medical Inc. 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 by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments. Ready to join a team thats 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 Sr. Quality Engineer will support manufacturing and work cross-functionally to resolve technical problems. Participates in decisions on scope of work risk management design changes process improvements material disposition and implementation of revised specifications. Provides and develops solutions to broad problems accomplishes complex assignments develops protocols for design and/or process activities (including those related to verification or validation activities) determines criteria and subsequently generates summary (or final) reports.

Essential Job Functions:

• Responsible for developing applying revising and maintaining quality standards for processing materials/products into partially or finished products.

• Designs and implements methods and/or procedures for inspecting testing and evaluating the precision and accuracy of products components sub-assemblies and/or production equipment.

• Analyzes nonconformance reports and returned products and recommends corrective action.

• Prepares documentation for inspection/testing procedures development studies validation protocols and reports quality plans product defect investigations and inspection plans. Must be able to write a technical document with sufficient clarity detail and correctness to be submitted for regulatory review with confidence. Must be able to review and provide value-added feedback to others writing such documents.

• Fully competent engineer in all conventional aspects of the subject matter functional area and assignments.

• Plans and conducts work requiring judgment in the independent evaluation selection and substantial adaptation and modification of standard techniques procedures and criteria. Provides guidance to manufacturing and development engineers regarding documentation process controls data feedback systems and best quality practices.

• Independently performs most assignments with an understanding of the overall expectations. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects.

• Plans schedules conducts and coordinates detailed phases of engineering work in part of a major project.

• Performs work which involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements unsuitability of conventional materials and difficult coordination requirements.

• Work requires a broad knowledge of precedents in the specialty area and a good knowledge of principles and practices of related specialties. Familiarity with FDA guidance documents and ISO and ASTM standards related to quality and medical device industry is an asset.

• Independently assesses if components sub-assemblies products meet specification and can initiate investigate and resolve non-conformances by working in conjunction with a multi-disciplinary team.

• Responsible for ensuring personal and company compliance with all Federal State local and company regulations policies and procedures for Health Safety and Environmental compliance.

• Responsible for participating in design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes and ensure the process has adequate and appropriate process controls. Responsible for participating and/or taking lead role in developing the risk management plan for new projects transitioning into manufacturing. (Hazard assessment design trace matrix development DV&V testing and FMEA).

• May technically supervise or coordinate the work of engineers technicians and others who assist in specific assignments.

• Practices company safety quality policies and procedures and actively requires conformance.

• May conduct internal and supplier audits. Certified as a lead auditor in ISO13485:2016 would be an asset. Familiarity with IEC 60601 and IEC 62304 is an asset.

• Processing investigating and completing customer complaints which could require direct email responses to customers.

• Composes technical complaint reports timely and accurately based on reported information and device investigation data.

• Responsible for developing and maintaining calibration requirements for tools and equipment in the R&D Manufacturing and Quality areas.

• Knowledge of statistics and Minitab including process capability and data normality assessments analysis of variance hypothesis testing determining appropriate sample sizes tolerance interval assessments for variable and attribute data design of experiment (DOE) and variable and attribute sampling plan applications would be a great asset.

• Other duties as assigned.

Requirements:

• BS in a related engineering discipline and 5 years of related experience; or MS in a related engineering discipline and 3 years of related experience

• Experience in the medical device industry is highly preferred

• Strong technical writing skills are required

• Experience in customer complaint investigations and complaint report writing

• Experience in manufacturing support as a Quality Engineer

• Must be proactive self-motivated and work independently with minimal supervision

• Experience with balloon catheters automated machines and electrical systems with software validation is strongly preferred

• Experience with Extrusion and Braiding is a plus

• Experience in completing Medical Device Reports (MDR) and Vigilance (MDV) submissions is an asset

• Experience in writing and reviewing design verification and validation protocols

• Preferred experience in generating documentation and criteria for validation of manufacturing line transfer to alternative sites

• Certification and/or license in a specific discipline would be an asset

• Certified Quality Engineer would be an asset

• Must be willing to travel up to 10% of the time

• Effective communication skills with all levels of management and organizations

• Operate independently and adaptability to changing requirements

• Ability to work in a fast-paced environment managing multiple priorities

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Analytical Reasoning Coaching Customer Centricity Data Savvy Document Management Financial Competence Good Automated Manufacturing Practice (GAMP) Lean Supply Chain Management Process Improvements Quality Control (QC) Quality Services Quality Standards Quality Systems Documentation Quality Validation Science Technology Engineering and Math (STEM) Application Supervision Supply Planning Technologically Savvy

The anticipated base pay range for this position is :

$91000.00 - $147200.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).



This position is eligible to participate in the Companys 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: - Experience:

Senior IC