Process Engineer
: Job Details :

Overview CORTLAND BIOMEDICAL - Who we are Cortland Biomedical custom builds high-performance biomedical textile structures. The company applies over 40 years of experience in textile engineering and advanced fabric design methods to braid, knit and woven products that meet the demands of a diverse set of customers in the biomedical product space. The company also offers a full range of design, development and manufacturing services as well as a wide variety of biomedical materials. Never comfortable with the status quo, complex biomedical textile challenges are tackled with agility, credibility and curiosity. Cortland Biomedical is wholly owned by Enerpac Tool Group. Enerpac Tool Group is a premier industrial tools and services company serving a broad and diverse set of customers in more than 25 countries. The Company's businesses are global leaders in high pressure hydraulic tools, controlled force products and solutions for precise positioning of heavy loads that help customers safely and reliably tackle some of the most challenging jobs around the world. The Company was founded in 1910 and is headquartered in Menomonee Falls, Wisconsin. Enerpac Tool Group trades on the NYSE under the symbol EPAC . For further information on Cortland Biomedical, visit the Company's website at For further information on Enerpac Tool Group and its businesses, visit the Company's website at Summary - basic function of the role Design and develop biomedical textile products and processes, manufacturing methods, techniques, practices and procedures with a focus on process development to ensure the manufacture of medical device component products which meet and exceed customer expectations. Shift: Monday - Friday; on-site Job Duties and Responsibilities Develop textile forming and finishing processes for new products in medical device applications. Support the development and documentation of detailed manufacturing processes to support new product development. Implement and optimize processes for manufacturing in a clean room environment. Create PFMEAs, EIOQs, Procedures, Work Instructions, Process Flows, Routers, and other QMS documentation in compliance with Cortland Biomedical QMS standards. Develop new technological solutions to manufacturing challenges including the use of digital tools for product documentation and traceability Write and execute engineering and validation protocols, to support process validations (IQ/OQ/PQ) and the creation of statistically derived product specifications. Responsible for the transfer of new product development processes to commercial production Support the creation, audit and review of test standards and methods for the analysis of design concepts and component assemblies. Support the identification, tracking, logistics and installation of capital equipment including potential travel for site acceptance testing. Support the design and manufacture of clean room compatible fixtures and tooling intended to aid manufacturing processes and interface with existing equipment. Expand Cortland Biomedical's expertise in state-of-the-art engineering, manufacturing methods and materials utilization through technical journals, seminars, advance degree programs, etc.