Johnson & Johnson
Santa Clara, CA
Shift: Full time
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: Supply Chain Engineering Job Sub Function: Manufacturing Engineering Job Category: Scientific/Technology All Job Posting Locations: Santa Clara, California, United States of America Job Description: Description - External Johnson Johnson is hiring for a Staff Manufacturing Engineer, Shockwave Medical 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 Staff Manufacturing Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production. The Staff Manufacturing 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 and Production departments to design, develop, test, document and implement processes, tooling, and fixtures. Collect data and analyze process performance and capabilities for company products, including new products and products already in production. Perform tolerance analysis for components, manufacturing materials, packaging, and supplies used for in-house processing. Lead effort to develop and maintains process Failure Modes and Effects Analyses (pFMEAs) for company processes. Prepare user requirements, technical specifications, and design specifications. Identify process requirements, advise and support operations management, and 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 other Quality System requirements. Evaluate existing engineering processes and implements process improvements. Lead and/or actively participate in product/process engineering problem solving using DMAIC methodology. Lead and/or actively participates in process/product improvement projects (in cooperation with production, R D engineers and technicians). Assist Procurement and R D departments with supplier selection and technical development. Recommend new technologies to improve system performance and reliability. Performs productivity and costing analyses (e.g., calculate direct labor, time studies materials costs for new and existing products), providing solutions that improve efficiency and scalability for years to come. Identify opportunities and implement cost reduction plans for existing products. Support the transfer of product lines and the qualification-validation efforts. 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. Qualifications - External Bachelor’s degree in Mechanical or Biomedical Engineering Minimum of eight (8) years of experience in a medical device environment or equivalent experience in other industries (pharmaceutical or automotive) that use the same principles of operation and similar regulations, or 6 years of experience with a Master’s Degree. Knowledge of and compliance with applicable Quality System requirements such as QSRs, FDA, ISO, MDD and other applicable regulations. Experience and understanding Process Validations (IQ, OQ, PQ), 6S, Lean Manufac