Urbana, IL, US
71 days ago
Processing Lead

KEDPLASMA provides a friendly and rewarding working environment with frequent opportunities for cross-training and advancement. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status.  

 

Please be advised that our organization participates in E-verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.  For more information on E-verify, please contact the Dept. of Homeland Security. 

 

 

Kedrion Biopharma & KEDPLASMA offer a number of benefits to qualifying employees, including: 

- Medical, vision and dental insurance 

- Life and AD&D insurance 

- Paid holidays 

- PTO accrual 

- and much more! 

Please let us know if you would like further details regarding the benefits that we offer to our qualifying employees, and we would be glad to provide you with our full benefits guide, as well as answering any questions you may have! 

 

Please note that salary ranges are calculated based off levels of: relevant experience, education and certifications. 

 
 

Duties and Responsibilities:  

1. Reviews donor record files to ensure completeness, accuracy, and compliance with cGMP.  

2. Assists in monitoring of inventory levels, management of the stockroom and opening and closing of lots for usage.  

3. Maintains cleanliness of work area to ensure a clean and professional environment.  

4. Communicates with management regarding pertinent information regarding work areas.  

5. Identifies areas of continuous improvement for his/her area of responsibility.  

6. Maintains cleanliness of work area to ensure a clean and professional environment.  

7. Maintains safety and integrity of product and samples during processing, storage and shipment release in accordance with Company DCOPs.  

8. Performs plasma and sample processing according to cGMPs, customer specifications, State and Federal regulations and Company policies.  

9. Possesses knowledge of the performance of sample centrifugation, label control, completion and inspection.  

10. Classifies and documents product according to donor programs.  

11. Provides support for casing, staging, quarantine and QA release of all products.  

12. As assigned, performs quality control on various laboratory equipment (e.g. freezer/refrigerator temperatures, Refractometer, HCT, PCS2 Machines, weight scales or other equipment).  

13. Manages product packing, and inventory within freezers for maximum efficiency. Controls disposition of unsuitable product with concurrent documentation.  

14. Prepares product shipment and verification.  

15. Receives inventory and maintains storage area for incoming supplies.  

16. Other duties as assigned by supervisor.  
 

JOB SPECIFICATIONS:  

1. High school diploma or equivalent.  

2. Available to work flexible and/or extended shifts.  

3. Occupational exposure to blood-borne pathogens.  

4. Demonstrated basic knowledge of computer equipment and software (DMS with training).  

5. Demonstrated accuracy in completing documentation.  
 

PHYSICAL REQUIREMENTS:  

1. Ability to sit or stand for extended periods of time.  

2. The employee is required to enter an environment with a temperature of -30C for short periods of time.  

3. Ability to tug, lift, and pull up to fifty (50) pounds.  

4. Be able to bend, stoop or kneel.  

5. Cold tolerance in storage freezers and adaptation to wide change of temperatures in handling samples and product.  

6. While performing the duties of this job, the employee is regularly required to stand; use hands to handle or feel objects, tools or controls.  

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