Manufacturing Engineer #41402

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Position Summary

At STERIS the Manufacturing Engineer is responsible for establishing and maintaining all manufacturing processes and procedures including capacity planning, tooling, process development, routings, cost reductions, and quality improvements in support of the Value Stream.  Shift schedule is 4-9 hour days and one 4-hour day.

What You Will Do - Manufacturing Engineer

•    Drives continuous improvement activities throughout the manufacturing processes. 
•    Develops fixture and/or machine designs to support production, improve processing, and implement production of new products. Typical processes include assembly, injection molding, and fastening operations (such as: pneumatic presses, adhesives, ultrasonic welding, resistance welding, and laser welding). 
•    Manages new and existing equipment installation and validation, including all required documentation in accordance with FDA and ISO standards. 
•    Assists with process control and troubleshooting. 
•    Establishes effective working relationships with multiple departments to maximize project management success. 
•    Develops and maintains costing documents for new products through direct labor standards and bill of material standard costs. 
•    Participates on and/or leads cross functional teams for the advancement of projects. 
•    Leads and implements cost reduction activities and capital equipment acquisition including payback analysis, capacity analysis, and business case justification.

•    Develops and maintains process documentation such that accurate documentation is provided at all times. Submits change orders to revise existing processes. 
•    Provides assistance in plant layout and ergonomics as needed such that products are produced efficiently while meeting ISO and industry standards.
•    Provides technical support and problem solving for production and facility problems.
•    Trains production personnel on new and revised processes. 
•    Works with quality and operations personnel to ensure ISO compliance. 
•    Provides Make versus Buy analysis for product components and tooling. 
•    Must be willing to be hands on and work closely with all levels of the organization. Requires most working hours to be in the manufacturing areas. 
•    Any other duties or projects as required.

What Will Help You Be Successful

•    Bachelor of Science degree required in an engineering discipline preferred with demonstrated technical experience. Will accept relevant co-op experience.   
•    Minimum eight years’ experience may be acceptable in lieu of degree.
•    Hands on experience in manufacturing setting 
•    Strong working knowledge of Microsoft Office software (Word, Excel, Access, & Outlook) 
•    Working knowledge of SolidWorks or similar CAD software 
•    Good written and oral communication skills required.
•    Lean manufacturing experience preferred.
•    Medical Device manufacturing experience preferred.
•    Experience in an ISO audited manufacturing company preferred.