Mgr Reliability Engineering at Johnson & Johnson in Irvine, CA

Mgr Reliability Engineering Location: Irvine, California, United States of America 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: Quality Job Sub Function: Quality Assurance Job Category: Professional All Job Posting Locations: Irvine, California, United States of America Job Description: RELIABILITY MANAGER: The Reliability Manager leads initiatives to ensure medical devices meet lifetime and safety expectations. The individual will analyze data to predict failures, drive corrective actions, and lead a team of engineers to build a "zero defect" culture. The role focuses on improving reliability through rigorous testing, data-driven analysis, and close collaboration with product teams, engineering, and suppliers to ensure parts meet performance standards and deliver long-term customer satisfaction. Responsibilities •    Develop and implement multi-year reliability strategies, including Design for Reliability (DfR) in R&D and post-market, to improve product robustness. •    Develop and implement early-life testing programs using engineering methodologies to identify components that may fail prematurely. ·       Oversee reliability testing, including environmental, thermal, shock, vibration, and lifecycle tests. Devises methods for inspecting and evaluating product precision. •    Apply statistical techniques and engineering analysis (Weibull analysis, regression, capability analysis) to evaluate failure data, detect early-life issues, and drive product quality improvements. •    Collaborate with R&D, product quality teams, and suppliers, leveraging statistical data analysis and engineering expertise to enhance medical device reliability during the early-life phase. •    Analyze large volumes of data, applying self-learning approaches to transform raw information into actionable insights. •    Serve as a single source of truth for data interpretation, collaborating with multiple teams to ensure consistent understanding. •    Ensure all products, processes, and documentation comply with FDA cGMP, ISO 13485, and other regulatory bodies. •    Lead a team of reliability engineers and technicians, partnering with R&D, manufacturing, quality, and regulatory teams. Requirements Bachelor’s degree in Mechanical, Biomedical, Electrical, or Reliability Engineering (Master’s or PhD preferred). Experience: 5–10+ years of reliability engineering experience in a regulated medical device or high technical R&D/Manufacturing environment. 3+ years of experience in a reliability management position Technical Skills: Strong knowledge of end-to-end reliability engineering and testing methods (HALT/HASS, accelerated life testing), statistical techniques. Familiarity with Reliability analysis tools such as Reliasoft, Minitab Familiarity with Data Analytics tools such as Tableau Strong collaboration and communication skills. Problem-solving and strategic thinking. Ability to lead cross-functional initiatives. Required Skills: Preferred Skills: Business Alignment, Coaching, Collaborating, Compliance Management, Continuous Improvement, Fact-Based Decision Making, Good Manufacturing Practices (GMP), ISO 9001, Process Improvements, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Quality Validation, Regulatory Environment, Standard Operating Procedure (SOP), Tactical Thinking, Technical Credibility The anticipated base pay range for this position is : $102,000.00 - $177,100.00 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