Material Handler

Country

United States

Shift

1st

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors.

Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Job Summary

As a Material Handler, you will be responsible for performing a variety of tasks involving the shipping, receiving, storing and distributing of materials, parts, supplies and equipment. Understand and comply with any/all guidelines within the Werfen Quality Manual, cGMP, GDP, FDA, ISO, Housekeeping, and Departmental Compliance.

Key Accountabilities

• Comply with all departmental procedures.
• Verify and process (data entry) for all deliveries according to cGMP and any/all departmental procedures
• Receives, handles, stores, rotates and delivers all raw material, components, finished goods according to FIFO, cGMP, and any/all departmental procedures
• Operates and maintains department equipment. Ensures that any inspections required are performed according to regulations.
• Identifies and helps troubleshoot incorrect performance of department equipment (where applicable).
• Warehouse work (storing/rotating supplies, raw materials/components, restacking pallets, and organizing storage areas.
• Perform cycle counts and/or physical yearend inventory (when required) of all supplies, raw material/components, Finished Goods and/or consumables.
• Pull/scan/pack orders according to FIFO, cGMP, and any/all departmental procedures.
• Identify and report any/all unsafe equipment and/or working conditions.
• Discard expired product when directed.
• Actively participates in the training of new employees.
• Perform other related duties as assigned
• Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

Networking/Key relationships

To be determined based on department needs.

Minimum Knowledge & Experience required for the position:

• High School Diploma or GED
• Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.

Skills & Capabilities:

• List Experience working in an aseptic (clean room) environment, preferred
• A Work Keys Silver Level ACT National Career Readiness Certificate (NCRC), preferred
• Ability to constantly use hands to place product on and remove product from wheel and visually check product
• Ability to use ladder to reach product/supplies
• Ability to maneuver Serum carts weighing approximately 700 pounds in and out of coolers
• Ability to stand over intervals of several hours at a time
• Ability to check for defects, check fill levels, and identify and distinguish between colors to help verify dropper assembly
• Ability to speak, read and write english
• Must be able to work irregular hours as necessary to meet production standards.
• Understand and follows FDA and ISO standards in accordance with Immucor Quality Manual, GEN, Quality Procedures such as cGMP and GDP, Good Housekeeping, and departmental…