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R&D Assembler II - Shockwave

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 Manufacturing

Job Sub Function:
Manufacturing Assembly

Job Category:
Business Enablement/Support

All Job Posting Locations:
Santa Clara, California, United States of America

Job Description:

Johnson & Johnson is hiring for a R&D Assembler II to join our team located in Santa Clara, CA.

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 R&D Assembler II is responsible for assembly, testing, and inspection of in-development, non-commercial product according to direction and documentation provided by R&D Engineers and/or Supervisor.

The R&D Assembler II records functions and activities performed on Lot History Records (LHRs) and other Quality Records, as appropriate.

The R&D Assembler II will also comply with documented requirements, company policies and procedures, including quality, safety, and environmental policies. 

 

Essential Job Functions


* Cleans workstations/equipment and performs line clearance per documented procedures.


* Builds prototypes, subassemblies, and/or final assemblies per MPIs or engineering documentation.


* Performs in‑process inspections of components/materials, subassemblies, and final assemblies to ensure that specifications are met for data collection and analysis.


* Uses documented guidelines provided by engineers and provides feedback for improved manufacturing methods to assist in the product development process. 


* Monitors equipment parameters and results of in‑process inspection(s); as necessary, adjusts according to documented procedures to ensure product meets appropriate quality specifications.


* Prepares labels, audits labeled product for product information per LHRs and assembles final product packaging.  Records and dispositions labeling materials used, destroyed, and leftover from packaging operations, as required.


* Ensures that only products...




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