Cantel Medical

  • Sr Manufacturing Engineer

    Location US-NY-Rush
    Job ID
    2019-5329
    # Positions
    1
    Category
    Engineering
    Company
    Cantel Dental
  • 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:
    Medical
    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.
    Dental
    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.

    #CB

    Job Overview

    The role will be a technical expert for Dental and will be responsible for improving production efficiency
    through processes, tooling and organizational improvements. The Senior Manufacturing Engineer will
    also be responsible for Project Management of Equipment and Automation.

    Main Responsibilities

    Lead/Develop Lean Engineering and Six Sigma Initiatives
     Establish engineering processes and appropriate documentation of equipment and processes
     Improve process capability and production volume while maintaining and improving quality
    standards.
     Development of Verification/Qualification deliverables including but not limited to Requirements
    Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary
    Reports.
     Execution of Test Protocols, including identification and resolution of nonconformances/deviations.
     Tracking and managing change control activities for multiple concurrent projects.
     Evaluate manufacturing processes by applying knowledge of product design, fabrication,
    assembly, tooling, and materials; conferring with equipment vendors and soliciting input from
    operators
     Root cause analysis/Risk Assessments performed to assure quality, safety, and delivery of
    products
     Document processes, test methods and, generate visual work instructions.
     Assure documentation and compliance with Quality Management System (QMS) and ISO
     Work with Quality organization to improve product and services
     Improve manufacturing efficiency by analyzing and planning work flow, space requirements, and
    equipment layout
     Develop project plans and execute on those plans
     Assure equipment parameters are established and met
     Lead the implementation of new product into production
     Other tasks as required and assigned
     Improve process capability and production volume while maintaining and improving quality
    standards.

    Qualifications

     B.S. in Mechanical Engineering, Manufacturing Engineering, or related field required.
     5+ years of experience in manufacturing environment required, preferably in medical device or
    other similarly regulated industry.
     Hands on experience working with Machinery required
     Knowledge of quality systems standards, such as, ISO 9000 and 13485, FDA CFR for medical
    device, pharma, or similar required.
     Proven success in leading continuous improvement efforts. i.e. 6S, Visual Management, Kaizen.
     Outstanding communication skills including listening, writing, and speaking.
     Ability to manage projects from inception to successful implementation.
     Strong Computer literacy, including Excel; CAD or SPC experience a plus.
     Ability to travel up to 25%

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