Manufacturing Process Engineer
STERIS - Mentor, OH

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Job Description:
Process Engineer
Job Description
Job Title: Process Engineer
Department: Operations – US Endoscopy
Reports To: Process Engineering Manager or Process
Engineering Supervisor
FLSA Status: Exempt
Prepared By: Human Resources
Prepared Date: March 27, 2013
Position Summary
Responsible for establishing and maintaining all
manufacturing processes and procedures including
capacity planning, tooling, process development,
routings, cost reductions, and quality improvements.
Essential Duties and Responsibilities include the
following. Other duties may be assigned.
Develop fixture 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).
Establish effective working relationships with multiple
departments to maximize project management success.
Develop and maintain costing documents for new products
through direct labor standards and bill of material
standard costs.
Participate in and lead cross functional teams for the
advancement of projects.
Lead and implement cost reduction activities and capital
equipment acquisition including payback analysis,
capacity analysis, and business case justification.
Develop and maintain process documentation such that
accurate documentation is provided at all times. Submit
change orders to revise existing processes.
Lead process validation activities for new or altered
processes in accordance with FDA and ISO standards.
Provide assistance in plant layout, ergonomics, and
process engineering such that products are produced
efficiently while meeting ISO and industry standards.
Provide technical support and problem solving for
production and facility problems.
Train production personnel on new and revised processes.
Work with quality and operations personnel to ensure ISO
compliance.
Provide Make versus Buy analysis for product components
and tooling.
Any other duties or projects as required.
Qualifications
To perform this job successfully, an individual must be
able to perform each essential duty satisfactorily. The
requirements listed below are representative of the
knowledge, skill, and/or ability required. Reasonable
accommodations may be made to enable individuals with
disabilities to perform the essential functions.
Competencies
To perform the job successfully, an individual should

demonstrate competency within the following areas:
Analytical Problem Solving
Project Management
Strong Interpersonal Skills
Attention to Detail
Teamwork
Sense of Urgency
Motivation
Dependability
Initiative
Innovation
Adaptability
Quality & Compliance
Education and/or Experience
Bachelor of Science degree required in Mechanical,
Biomedical, Industrial, or Manufacturing Engineering.
5 Year+ experience in a process, industrial, or
manufacturing engineering capacity
Strong working knowledge of Microsoft Office software
(Word, Excel, Access, & Outlook)
Working knowledge of AutoCAD and/or SolidWorks
Good written and oral communication skills required
Lean manufacturing or six sigma experience is a plus
Medical Device manufacturing experience will be a plus
Experience in an ISO audited manufacturing company a
plus
Physical Demands
The physical demands described here are representative
of those that must be met by an employee to successfully
perform the essential functions of this job. Reasonable
accommodations may be made to enable individuals with
disabilities to perform the essential functions.
Occasionally may need to lift and carry a 25 lb. bin as
far as 25 ft.
May be required to stand and walk for majority of the
shift.
Please see above job description for a list of all
requirements.

Steris - 16 months ago - save job - block
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About this company
18 reviews
STERIS Corporation (STERIS), together with its subsidiaries, develops, manufactures, and markets infection prevention, contamination...