Experience Requirements
5-10 years of experience in manufacturing engineering, in process development, with stainless steel, small component design and mechanical assemblies.
Qualification Requirements
BS Mechanical Engineering, or the equivalent in a related field.
Preferred Qualifications
Experience in medical industry a plus.
Responsibilities
The Sr. Process Engineers is responsible for the design and development of new prototype development products and technologies, for new product concepts, including design calculations, creating solid models, and detailing prints with minimal supervision, and for interfacing with customers, suppliers, R&D and manufacturing, all of which are essential to achieving our goal of on-time delivery and high quality products.
MAJOR DUTIES AND RESPONSIBILITIES:
Develop and execute complex projects which encompass design, development, and implementation of new products and technologies.
Use of SolidWorks (3D Modeling) and CAM programs to create designs and drawings
Research new materials, assembly methods, and manufacturing processes
Initiate, process, and review Engineering Change Notices
Provide support to R&D, manufacturing, marketing, and customer service; interface with customers and suppliers
Manage projects in a matrix organization as a team leader, whose duty encompasses the full scope of the project
Determine product specifications/limitations
Assist with the design of gages, fixtures, and tooling
Support design and process FEMA’s
Review routings and add additional information to prints as required
Perform analysis verification of design, which may include calculation and/or FEA
KNOWLEDGE / SKILLS
Use 3D Modeling, preferably SolidWorks
Proficient in designing, acquiring, and implementing new equipment and processes.
Good working knowledge of manufacturing methods, including RF plastic forming, injection molding, and assembly methods
Knowledge in plastics processing, tooling and materials.
Experience with lean manufacturing
Proficient in MS Office Products
Experienced in process controls
Excellent oral and written communication skills
Ability to prioritize and work independently
Familiar with the design controls, FDA regulation, and GMP practices
Experience with risk analyst
Relies heavily on experience and judgment to plan and accomplish goals
Good working knowledge of GD&T.
Ability to prioritize and work independently.
