Material Handler
Werfen
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.
Job description
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.
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:
- Experience working in an aseptic (clean room) environment, preferred
- A WorkKeys 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 compliance in general.
- Displays ability to be an effective team member.
- Maintain a clean and neat work environment.
- Interacts cooperatively with coworkers & receives direction well from Management.
- Meets achievement levels established for error accuracy rates and competency evaluations
Requirements
- High School Diploma or GED
- Experience working in an aseptic (clean room) environment, preferred
- A WorkKeys 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 compliance in general.
- Displays ability to be an effective team member.
- Maintain a clean and neat work environment.
- Interacts cooperatively with coworkers & receives direction well from Management.
- Meets achievement levels established for error accuracy rates and competency evaluations
Company overview
Werfen is a global leader in specialized diagnostics, founded in 1966 in Barcelona, Spain as a family-owned innovative company. The organization has established itself as a worldwide authority in five key clinical areas: Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant diagnostics. With headquarters in Barcelona and technology centers strategically located in the United States and Europe, Werfen operates directly in 30 countries and serves more than 100 territories through distributors. The company achieved remarkable financial performance with worldwide sales exceeding €2.2 billion in 2024, supported by a workforce of over 7,000 employees globally. Werfen's comprehensive portfolio includes advanced diagnostic systems, reagents, laboratory automation solutions, and point-of-care testing platforms that enable healthcare providers to deliver precise and timely patient care. Their innovative technologies span from blood gas analyzers with hemolysis detection capabilities to automated immunoassay systems and specialized diagnostic assays. As a vertically integrated diagnostics company, Werfen maintains complete control over research, development, manufacturing, and distribution, ensuring quality and reliability across their product lines while continuously advancing diagnostic science to address critical healthcare challenges worldwide.