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. Duties Is responsible for daily set up and operation of the complete filling and packaging lines consisting of the sponges, pouches, vials, caps, labels, inkjet code dater and check weights in accordance wi

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. The Role The Health Safety & Environment (HSE) Engineer at the STERIS V. Mueller facility in St. Louis is primarily responsible for assisting the V. Mueller HSE department in the development and maintenance

The Supply Chain Manager is responsible to provide leadership in procurement activities for the site, including inventory control and material flow. You will develop and execute strategies within a lean environment concentrating on talent leadership, Customer experience, Risk management and Cash Generation. You will be responsible for both tactical daily execution of mate

Setup and operate Computer Numerically Controlled (CNC) lathes and/or mills. Primarily responsible for setting up and operating equipment with some program editing and offsetting on a variety of parts. Responsible for meeting dimensional requirements. Shifts 3 00pm 1 30am Monday Thursday Benefits Healthcare, Vision, Dental, 401K Match, Quarterly Bonuses, PTO, Company Holi

At STERIS, the QC Laboratory Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards.The QC Laboratory Specialist is responsible for performing quality inspection in accordance with the requirements for ISO, FDA

The VP of Quality is responsible for leading manufacturing sites in the execution of the overall STERIS Quality System for the Consumable product portfolio. This position is principally responsible for identifying and implementing strategies to improve product and ensure sustainable product Quality. In addition, this role has responsibility for driving product and process

STERIS has an excellent opportunity for an experienced Senior HR Generalist. This role will support our St. Louis site, a showcase plant with our manufacturing and chemical packaging teams. Additionally this role will supportthe St. Louis Distribution Center. The Senior HR Generalist partners with managers and employees at various levels to provide HR support and solution

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. The Role The Manufacturing Supervisor in the STERIS St. Louis, MO facility leads teams of employees in the tasks related to the efficient production of STERIS, St. Louis Operations products. Responsible for

The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Quality Technician supports manufacturing and servicing operations by assisting in performing and documenting problem solving investigation

To support manufacturing operations and produce quality product with efficiency and accuracy. Shift 3 00pm 1 30am Monday Thursday Benefits Healthcare, Vision, Dental, 401K Match, Quarterly Bonuses, PTO, Company Holidays Duties Performs a variety of operations to meet specified dimensions and tolerances based on manufacturing documents including part prints, process router

The Value Stream Manager (Production Manager) is responsible for achieving annual objectives for safety, quality, delivery and cost of the assigned value stream or defined area. You will embrace Lean transformation through education of self and direct reports, kaizen concepts and activities, visual management tools, and root cause problem solving. Works closely with the D

Duties Duties cont'd Education Degree Required Experience STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE

The Senior QC Laboratory Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role is responsible for generating test methods, reports, and specifications for raw material, in process, and finished goods

The Senior QC Laboratory Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role is responsible for generating test methods, reports, and specifications for raw material, in process, and finished goods

IMS Technicians Device Repair perform surgical instrument and device inspection, repair, and refurbishment in a lab based setting. This role delivers superior Customer Experience by providing timely and quality repairs to meet compliance standards in a production facility as part of a high performing team. Pay $21/hour + skills based incentive program, yearly merit increa