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.
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.
Work with Cantel Medical Product Development team to execute risk based
approach/procedure/plan to develop/design requirements/specifications, technical
standards, test methods, test plans, test protocols and test data analysis.
Responsible for the identification of technical standards against QSR, EPA, EU MDD and other
target market regulatory and clinical requirements.
Responsible for partnering with Product Development teams and Supply Chain personnel in
the assessment of component and system level specifications relative to customer needs and
product performance specifications.
Apply Design for Reliability and Manufacturability tools and techniques to ensure Cantel
product designs are robust, fit Cantel’s manufacturability model, and meet customer needs.
Provide effective Quality Engineering support for multiple projects, balancing priorities and
resources appropriately to meet both project and management expectations.
Collaborate with R&D, Marketing, Regulatory Affairs, Supply Chain and Manufacturing to
ensure effective and robust risk management, testing, verification, validation, IQ/OQ/PQ as
applicable for products and processes in the concept to market phases of product
Assist in continuous improvement activities as necessary and as driven by product lifecycle
management that generate Sustaining Engineering projects.
Prepare oral and/or written reports of analysis for Design Verification, Design Validation and
other critical testing and evaluation activities, as required by the project or department
Update job knowledge by keeping abreast of trends and developments in design quality
assurance, statistical analysis, test development, ISO 13485, MDD, TGA, Health Canada and
FDA quality systems, and participating in educational opportunities.
BS degree required, Diploma holder in Engineering or Physics
3 plus years Design Quality Assurance experience in a regulated medical device
environment, specifically in a product development support role
Experience in responsibility for compliance to FDA, MDD and ISO regulations
Experience in responsibility for medical device Design Verification and Validation activities
Experience in and responsibility for product and process risk analysis/FMEA, specification
writing, test method development, statistical analysis of quantitative and qualitative data,
test report writing and medical device design reviews.
Previous work experience in life science products or medical device fields is required
Proficient in computer skills such as MS office programs
IDEAL CANDIDATE PROFILE:
Strong written and oral skills
Strong organizational and management skills
Strong problem solving skills
Strong attention to detail