Cantel Medical

  • Process Development Engineer

    Location US-MN-Plymouth
    Job ID
    # Positions
    Cantel Medical
  • Company Overview

    At Cantel, preventing infection is our business. We are dedicated to delivering high-quality, innovative solutions that help our customers improve patient care. Choosing a career with Cantel means joining a company that’s driven by an entrepreneurial spirit and the passion to shape the future of infection prevention. If you want to be inspired by your work and have a hand in shaping the future of infection prevention, we want to meet you. Come and see why people love working here.
    Cantel is a leading global company dedicated to delivering innovative infection prevention products and services for patients, caregivers, and other healthcare providers which improve outcomes, enhance safety and help save lives. Our products include specialized medical device reprocessing systems for endoscopy and renal dialysis, advanced water purification equipment, sterilants, disinfectants and cleaners, sterility assurance monitoring products for hospitals and dental clinics, disposable infection control products primarily for dental and GI endoscopy markets, dialysate concentrates, hollow fiber membrane filtration and separation products. Additionally, we provide technical service for our products. Cantel medical is a leading provider of infection prevention products and services in the healthcare market, specializing in the following operating units:
    Endoscopy procedure disposables include single-use valves and irrigation tubing. Medical device reprocessing systems, disinfectants, detergents and other supplies are used to disinfect high-level endoscopes. This segment is operated through MEDIVATORS.
    Life Sciences
    Water purification systems for dialysis facilities, including hemodialysis dialyzer and reprocessing systems, as well as sterilants and filtration products. This segment is operated through Mar Cor Purification, Inc. and MEDIVATORS.
    Single-use, infection prevention products used primarily in the dental market including face masks, sterilization pouches, towels and bibs, tray covers, saliva ejectors, germicidal wipes, plastic cups and disinfectants. This segment is operated through Crosstex International, Inc.


    Job Overview

    The Process Development Engineer will be Operation’s champion during the development stages of new products
    and line extension activities. This will include manufacturing development and readiness for a variety of medical
    devices with a focus on hollow fiber filters. The Process Development Engineer will lead the manufacturing process
    development, provide DFM feedback, develop equipment requirements and specifications, lead design transfer
    builds, and ensure all processes are validated

    Main Responsibilities

     Support line extension activities focused on improving the manufacturing of hollow fiber filters.
     Ensure that operations requirements are incorporated into designs during product development.
     Develop advanced manufacturing systems and processes to with a high level of operational quality to
    ensure process capability, repeatability & reproducibility in launched product
     Participate within cross functional NPD team activities such as Design for Manufacturability and Assembly
    (DFMEA), Design Reviews, pFMEA, etc.
     Lead and coordinate operational readiness and design transfer activities at manufacturing sites.
     Lead project planning with manufacturing locations to determine manufacturing operational requirements
    including capacity, space, processes, and detailed equipment requirements.
     Lead preparation and execution of process readiness reviews with stakeholders to demonstrate
    operational readiness including process and equipment validations.
     Lead development of manufacturing lines utilizing lean manufacturing concepts.
     Assist in the improvement and development of new product development processes to enhance
    development of robust products while reducing time to market.
     Ability to travel 10%, occasional travel to customers or suppliers as required.


     BS in Engineering, preferably Mechanical Engineering or Chemical Engineering.
     Minimum of 5 years of engineering experience.
     Experience in Design for Manufacturing & Assembly, DFMEA, PFMEA, DOE, and Validations.
     Experience in Process Development.
     Experience with hollow fiber filter manufacturing
     Experience in the medical field or other regulated industry
     Familiar with ISO 13485 and FDA Design Control.
     Green Belt Certification
     Project planning skills.


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