Johnson & Johnson, Quality Engineer 1 NPD - Application via WayUp

This role is with Johnson & Johnson. WayUp is partnering with Johnson & Johnson to hire top talent.

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

• Job Function: Quality
• Job Sub Function: Quality Assurance
• Job Category: Professional
• All Job Posting Locations: Irvine, California, United States of America
  
  

Job Description:

• About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at
  
  

We are searching for the best talent for Quality Engineer 1 NPD to be in Irvine, California . The NPD Quality Engineer 1 executes quality assurance activities intended to ensure effective product quality processes are in place and executed throughout the lifecycle of a product. Involved in NPD teams and other activities to develop products, design verification tests, process validations and quality processes to ensure compliance with the company’s Quality System policies and procedures and applicable external requirements and standards. As needed, assists in developing quality-engineered systems and products, and support qualification and validation activities. Will show leadership in driving program/projects and innovating compliant approaches and solutions to problems. A few of the responsibilities may involve collaborating with other members of the Design Team. Will contribute to activities including risk management document development, creation, and design of catheter test methods, authoring of test protocols, and testing of products during their development cycle. If you are an individual who enjoys working with the other team members and changing the lives of our patients around the world, come join our team!

Key Responsibilities:

• Provide support in quality improvement opportunities as appropriate to new products, continuous improvement and customer satisfaction.
• Understand the investigation processes related to corrective and preventive action (CAPA) as well as nonconformances (NC), identification of root cause and recommend action(s). Generate nonconformance reports and assist in investigation, final disposition and corrective action.
• Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE).
• Assign/review quality inspection testing and test data. Communicate activities and issues to supervisor.
• Reviews documents for GDP.
• Support audits.
• Help execute and develop process and product validation/verification protocols and reports, equipment qualifications and engineering change orders. Qualifications Education:
• A minimum of a Bachelor’s degree with focus in engineering and/or scientific field is preferred. Alternatively, 2+ years of quality, manufacturing, or research and development experience in a medical device or other regulated industry. Experience and Skills: Required:
• Ability to define problems, collect and analyze data, establish facts, and draw conclusions and recommendations
• Ability to effectively collaborate and connect with internal and external partners at all levels of the organization including influencing and negotiating resulting in positive business and quality outcomes
• Ability to function in a team environment and deliver on team objectives
• Strong attention to detail Preferred:
• Familiarity with general quality management system concepts, including good documentation practice (GDP), corrective and preventive action (CAPA), and document change control practices.
• Developed presentation skills.
• Understanding of theoretical and practical fundamentals and experimental engineering techniques such as DOE, DMAIC and ANOVA.
• Working knowledge of SolidWorks, other CAD based programs (i.e., basic dimensioning, tolerance stack analysis).
• Experience with Minitab, R and other statistical software.
• Six Sigma or lean manufacturing experience, and/or knowledge of Process Excellence tools.
• Experience in Class III medical devices and/or cardiac products Other:
• This position may require up to 20% of domestic and/or international travel. Additional Information: The expected base pay range for this position is $28 - $40/hr.
• The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.
• This position is overtime eligible
• Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
• Employees may be 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.
• Employees are eligible for the following time off benefits: o Vacation –120 hours per calendar year o Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year o Holiday pay, including Floating Holidays –13 days per calendar year o Work, Personal and Family Time - up to 40 hours per calendar year o Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child o Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member o Caregiver Leave – 10 days o Volunteer Leave – 4 days o Military Spouse Time-Off – 80 hours
• Additional information can be found through the link below.
  
  

This job posting is anticipated to close on June 17, 2025. The Company may however extend this time-period, in which case the posting will remain available on to accept additional applications 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 (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource

• The anticipated base pay range for this position is : $28 - $40/hr
  
  

_Additional Description for Pay Transparency:_

Johnson & Johnson is a healthcare company that develops medical devices, pharmaceutical, and consumer packaged goods.