INGENYX - Engineer III, Development

Expected Travel : Up to 25% Requisition ID : 14274   Ingenyx proudly launched as a new, independent company following its divestiture from Teleflex on August 3, 2026.   Ingenyx is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fibers; and bioabsorbable sutures, yarns and resins. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.   For more information, please visit  Ingenyx.com Position Summary

The Engineer III, Development is responsible for leading the execution and oversight of engineering projects of varying complexity within the OEM Performance Fibers (sutures) business unit. With a focus on new development projects such as sterile and non-sterile line extensions, new suture constructs, processes and technologies, they are responsible for leading and supporting Development projects with a low level of guidance. They are also responsible for establishing and supporting manufacturing operations including the validation of new equipment and materials, troubleshooting development processes, as well as identifying and implementing process/product improvements within development activities. The engineer will work with cross-functional teams to, resolve material issues, customer complaints, design and develop new product, and review potential new business opportunities. The Engineer III, Development is expected to have a working proficiency in Design Control and development methods, medical device regulations, manufacturing, and project management. They will be expected to successfully carry out and support project deliverables/product development functions with a focus on quality, compliance, and customer needs.  The scope of products for which the Engineer III, Development will be primarily responsible for developing and supporting includes sterile and non-sterile suture components, contract manufactured suture products, and sterile suture devices for the Mansfield, MA, Coventry, CT, and Nuevo Laredo, MX facilities.  Principal Responsibilities

•    Plan, lead and manage projects and manufacturing engineering activities of moderate to low complexity independently. Manage complex projects/programs with some guidance.  •    Lead development of products that minimize/mitigate product and manufacturing variation, scrap rates, and productivity throughout the manufacturing process, from supplier management to distribution of product. •    Develop custom devices, sutures and subassemblies according to customer design, performance, and quality specifications; on time and within project constraints. •    Identify and manage the scope of projects with a good understanding of interdependencies. •    Draft and route project initiation/closure documents, identifying the required deliverables per local and global procedures, as well as governing regulations, with minimal guidance based on project complexity. •    Interface with cross functional teams to maintain accountability, coordinate and execute deliverables supporting new product and capability development projects, and other initiatives.  •    Serve as central contributor to identification and execution of continuous improvement initiatives. •    Accurately predict project requirements, costs, lead times, and delivery schedules during the quoting and project execution processes. •