Hiring: INGENYX - Engineer III, Development Company: Teleflex Location: Mansfield, MA Job Posted Time: 2026-09-10 14:19:05 Employment Type: Contract Target Skills & Keywords : Assembly, Epic Systems, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Project Management, Quality Assurance, Regulatory Compliance, Root Cause Analysis About the job Experience: •4 years of experience in medical device or related field (5+ years preferred). •4 years of experience successfully leading projects and/or project deliverables (5+ years preferred). •Minimum 4 years of experience in medical device or related field (5+ years preferred). Required Skills: •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. •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. Qualifications: •Bachelor of Science in an Engineering or related technical discipline. •Minimum of 4 years of experience successfully leading projects and/or project deliverables (5+ years preferred). •Knowledgeable in U.S. FDA GMP and ISO requirements for the design, validation, and manufacturing of medical components and/or devices. •PMP certification is a plus. •Support and lead root cause analysis investigations, NC’s and CAPA’s and customer or project related problem resolution activities. •Coordinate and support proper creation and maintenance of drawings, procedures, design documents as well as other technical and manufacturing documentation. •Assist in establishing continuous improvement initiatives and methods of application. •Utilize understanding of medical device development and product line fundamentals to develop project strategies of moderate complexity. •Contribute to creation/remediation of new processes, methods and techniques. •Ensure projects are developed and documented compliant with the Quality System. Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!