Staff Metals Development Engineer

Johnson & Johnson•Santa Clara, CA

37d•$91,000 - $165,050•Onsite

About The Position

At Johnson & Johnson,â¯we believe health is everything. Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯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.â¯Learn more at https://www.jnj.com We are searching for the best talent for Staff Metals Manufacturing Development Engineer located in Cincinnati, OH! About MedTech: Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, and more personalized treatments. Your outstanding talents will help patients on their journey to wellness. Learn more at Johnson & Johnson MedTech Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. The J&J Supply Chain is an integrated, global supply chain that serves the needs of the 1 billion people who use J&J products each and every day around the world. We manufacture more than 26 billion product units per year, from raw component sourcing to end product distribution as efficiently and effectively as possible with high quality, compliance and service performance. Our supply chain organization makes up 45% of all J&J employees, and includes 125 internal manufacturing plants, manages 581 external manufacturers, utilizes 459 distribution centers, partners with over 3700 direct suppliers, produces over 300,000 sku's. Overview and Key Responsibilities: The Staff Engineer will join a team of leading specialists in world-class manufacturing technologies to lead a technically specified project portfolio impacting the entire MedTech sector of companies. This individual will be ambitious to bring innovation, customer access, supply reliability, and cost down initiatives to the market. In addition to delivering launch excellence in new product innovation through multi-functional partnership, supplier collaboration, and robust technical strategies.

Requirements

Bachelor of Science in Engineering
A minimum of 6 years of related work in a regulated industry
Validated knowledge of various metal component manufacturing processes development and production validation (ie. machining, metal injection molding, stamping, casting, coining, EDM/ECM, additive manufacturing, etc.)
Awareness of design for manufacturability and assembly standard methodologies for metals processes and design requirement cascade for instrument and implant manufacturability
Ability to interpret engineering drawings, and create robust metrology strategies
Understanding of tolerance stack-up analysis and GD&T
English fluency required
The position requires you to be on site 3 days/week minimum

Nice To Haves

Technical writing and basic project management methodologies
Advanced digital literacy and use of software applications.
Experience in a manufacturing/production environment
Process Excellence Practices including MSA, GR&R, DOE, process characterization, process capability
Adaptable to shifting priorities according to changes in organizational needs
Strong organizational, interpersonal, oral, and written communication skills.
Experience in medical grade materials

Responsibilities

Explore, design and drive technology & equipment selection, development, and deployment of solutions for various metals processes
Function as an integral member of a team in support of manufacturing operations performed by external manufacturers, providing technical services to ensure quality, cost and performance objectives are met.
Apply engineering principles, world-class manufacturing techniques, statistics, and risk management to resolve complex technical challenges.
Developing talent through coaching and mentoring
Lead root cause investigation and corrective actions to address manufacturing yield or capacity issues
Proposes and determines new or improved technologies, processes, or materials to enhance product quality, manufacturing cost efficiencies, portfolio pipeline, and regulatory compliance
Provide engineering expertise to critical internal and external business partners to influence product capital strategy to meet current and future capacity needs
Demonstrate independent understanding and application of core GMP fundamentals, including, but not limited to: Data Integrity (DI), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDPs)
Coordinate project activities and maintain accountability for overall project success
Communicate business related issues or opportunities to next management level.