Mathieu Joseph Email & Phone Number

Naples, Fl, Us

Naples, Florida, Us

Responsible for the strategic oversight and management of suppliers for both sterile and non-sterile electromechanical devices, ensuring optimal performance, adherence to regulatory standards, and the continuous improvement of supply chain efficiency and product quality.

Naples, Florida, Us

- Collaborate closely with design engineering and manufacturing teams to establish comprehensive design requirements and formulate effective manufacturing processes in alignment with new product development initiatives.- Lead efforts in quality assurance, control, and proactive measures to drive enhancements in internal products and operational processes, contributing to sustained product excellence.- Demonstrate expertise in identifying and resolving supplier quality challenges, ensuring seamless daily operations and minimizing inventory disruptions.- Continuously play a pivotal role in fostering a culture of continuous improvement by implementing strategic initiatives that optimize internal procedures, resulting in enhanced product quality and streamlined processes.

Naples, Florida, Us

Palm Beach Gardens, Fl, Us

In my current role, I am responsible for supporting design and development projects and assuring the design process meets all applicable QA requirements. In addition, I am responsible for reviewing design drawings for tolerance, risk management files, inspect-ability and quality of design issues, work with suppliers to improve quality and assist, where necessary, in supplier qualification and supplier process validations. Lastly, I am responsible for assisting in the design and development of methods and tooling for the test and inspection of articles.

Warsaw, Indiana, Us

Current job function includes:-Provide QA support to R&D for new and existing products-Responsible for design FMEA activities on the project, supplier qualification/evaluation and communications until design transfer

Boston, Ma, Us

Fort Lauderdale, Fl, Us

● Developed and executed validation protocols and test methods pertaining to the manufacturing process of orthopaedic products

Doral, Fl, Us

● Generated validation protocols and reports for Infusion Pump equipment● Performed Root Cause Analysis on RubigenTM Generator● Facilitated target completion date with appropriate personnel from other departments● Performed equipment qualification and maintenance to ensure compliance with the FDA.● Participated in process design and development activities

● Worked with university engineering team to create a Remote Accessory for Medtronic NavigusR KitResearch Project● Responsible for research on Biomaterial Validation Laboratory Protocols● Researched and analyzed test protocols for compliance to standard test methods● Performed cost assessment of the project● Interacted with R&D, and manufacturing departments to evaluate/critique the design proposal

Master'S Degree, Regulatory Affairs For Medical Devices, Pharmaceuticals, And Biologics

Bachelor Of Science (Bs), Biomedical Engineering

Associate Of Arts (Aa), Biology/Biological Sciences, General