Material Handler II

Steris Corporation•Libertyville, IL

62d•Onsite

About The Position

The Material Handler I is responsible for the safe movement of Customer products. Safely and accurately process routine and moderately complex Customer products according to established specifications and procedures within FDA, ISO and GMP guidelines using work instructions and operating system knowledge. Depending on the modality in which this role operates (i.e. Gamma). This is a highly physical role – requiring strength and endurance. Shift Hours: Night shift (7:30 pm-7:30 am) rotating days. Pay: $21.75 with a $2 Shift Differential as applicable

Requirements

High School Diploma or GED.
Having the ability to lift up to 50lbs.
Ability to effectively read, write and verbally communicate.
Ability to work independently under general guidelines and supervision.
Requires the ability to navigate through defined computer screens.
Requires effective interpersonal skills as demonstrated through prior experience.
Able to adapt to changing duties and responsibilities.
Normal hearing range sufficient to hear alarms, bells, horns, etc.

Nice To Haves

A minimum of two (2) years of warehousing/manufacturing experience.

Responsibilities

Transfers product from unprocessed storage area to processing area, loads, and unloads processed product, conducts pre-shipping preparation and stages product in processed area.
Reviews product / process documents and customer provided special instructions to ensure accurate processing.
Maximizes processing and minimizes downtime by monitoring equipment used for product movement and transfer; conducts and performs minor repairs, referring major malfunctions and / or unsafe conditions to management or Maintenance Department; maintains a clean orderly work area, performs Material Handling, production functions as needed.
May assist in maintaining product inventory by receiving, identifying, labeling if appropriate, and storing product within the Shipping and Receiving area in accordance with established procedure and any applicable Customer provided special instructions.
Contributes to accuracy of processing and product accountability by maintaining product documentation; implements appropriate corrective action as needed; places, retrieves and analyzes product monitoring devices per processing specifications.
Contributes to a team effort by performing in accordance with all STERIS policies, GMP, Lean principles and other directives; supports the directives and decisions of higher-level management.
Other duties as assigned.