Mechanical Engineer II

Enerpac Tool Group Corp•Munsons Corners, NY

5h•$86,330 - $129,500•Hybrid

About The Position

Design and develop biomedical textile products and processes, manufacturing methods, techniques, practices and procedures with a focus on component processing to ensure the manufacture of products which meet and exceed customer expectations.

Requirements

BS Degree in Mechanical, Textile or Biomedical Engineering from an accredited university
3+ years of experience in an engineering function within a manufacturing environment - especially in highly regulated industries (medical, energy, aerospace, automotive, etc.).
Familiar with the physical and mechanical characteristics of polymers, fibers, yarns and fabrics a plus
Effective verbal communication skills and comfortable interacting with team members and customers at all levels
Effective technical writing skills consistent with writing engineering reports and quality management system documentation.
Must have demonstrated creative problem solving and effective engineering decision making skills.
Demonstrated ability to work well independently and as a team member
Self-starter able to work under minimal supervision
Capable of generating and delivering presentations to management, peers and labor force
Ability to communicate effectively, develop relationships, adapt, be customer focused, and innovate.

Nice To Haves

Experience with Enterprise Resource Platforms (ERP) preferred
Demonstrated proficiency of design software such as AutoCAD or SolidWorks a plus

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.
<10% domestic and international travel in support of customers, engineering projects, site acceptance tests and training