Join Steris as Process Engineer in St. Louis Missouri. At the Steris you will perform tasks as listed below, Apply Steris Manufacturing Operations careers in St. Louis MO.
Position : Process Engineer
Job Category: Manufacturing Operations
Work location : St. Louis, Missouri
Job Segment : Chemical Research, Manufacturing Engineer, Process Engineer, Project Engineer, Chemical Engineer, Engineering
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.
Provides technical expertise to a liquid blending and packaging operation to improve safety, identify and eliminate the ro0t causes of defects, shorten lead times and lower costs. Monitors process data to identify and solve problems and propose kaizen activities for improvement. Leads cross-functional kaizens and capital equipment specification, modification and replacement as needed to meet Safety, Quality, Delivery and Cost objectives.
Develop and manage the execution of validation protocols to meet FDA and cGMP requirements for equipment and process qualifications.
Optimize new and existing equipment and processes using Kaizen Methodology, 5S, TPM, Single Piece Flow, Quality at the Source, Single Changeover, and other Lean Manufacturing tools.
Interfaces with Product Development and Production to move new and reformulated products and processes from the lab through scale-up into full-scale manufacturing.
Supports Project Engineering to obtain approval for Capital Appropriation Requests, design specifications and equipment installation. Provide personnel training, development of manufacturing instructions and start-up of new processes/equipment.
Resolve nonconformances. Document root cause and lead the implemntation of corrective and preventive actions.
Develops and submits written reports including, objective, experimental, compilation of data, engineering analysis, conclusions and recommendations.
Bachelor’s Degree in Chemical Engineering
Three to five years’ experience in process engineering, production support and/or batch chemical processing.
Project management, technical and organizational skills required.
Familiarity with current Good Manufacturing Practices (cGMPs) and familiarity with FDA regulations preferred. Good communications and interpersonal skills needed.
STERIS is a leading provider of products and services that meet the needs of growth areas within Healthcare: procedures, devices, vaccines and biologics. We exist to fulfill our MISSION TO HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD. STERIS is a $3B, publicly traded (NYSE: STE) company with approximately 16,000 associates and Customers in more than 100 countries.
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.
Nearest Major Market: St Louis
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