Job Description
Processing Lead
Posting Start Date:  5/1/25
State/Province:  Texas
Job Location:  Palmview
Place of Employment: 
Contract Duration:  Permanent
Hiring Pay Range Min:  16.00
Hiring Pay Range Max:  18.00
Processing Lead

KEDPLASMA is a subsidiary of Kedrion Biopharma Inc. KEDPLASMA specializes in the collection and procurement of high-quality plasma that is processed into plasma-based therapies Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help treat and prevent serious diseases, including Hemophilia, Primary Immune System Deficiencies, and Rh-Sensitization.


Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.


Salary ranges are determined based on relevant experience, education, and certifications.
If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at kedtalent@kedrion.com.


Employee Benefits
At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including:

  • Health & Wellness – Full medical, dental, and vision coverage
  • Financial Security – Life insurance, AD&D, and retirement savings plans
  • Work-Life Balance – Paid time off, sick leave, and paid holidays
  • Career Growth – Training programs and development opportunities
  • Extra Perks – Employee discounts, wellness initiatives, and more!

For specific inquiries please reach out to us

Responsible to ensure accurate and timely processing of unit sampling, storage and compliance of plasma collected from donors while providing oversight of plasma inventory and shipments including submission of sample testing and backup samples, medical supplies and soft goods inventory levels, and Specialty Programs (where applicable) under the direction of the Center Manager. Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR.

 

  • Performs sample centrifugation, label control, completion, and inspection.
  • Prepares equipment by performing PQ/calibrations and verifying required maintenance has been performed as outlined in the SOPs.
  • Performs plasma and sample processing according to cGMPs, Customer Specifications, State and Federal regulations and company policies.
  • Responsible for aseptic sampling and heat sealing of plasma units and timely placement of units/samples into freezer per SOPs to ensure product quality.
  • Performs troubleshooting of equipment within scope of training.
  • Alerts management when equipment poses a risk to donor/product safety.
  • Troubleshoots equipment failures, including proper diagnosis and documentation of events to include removing and/or returning equipment to service.
  • Ensures only one plasma unit and samples are properly labeled at a time and performed within the areas of unidirectional flow designated for each task according to SOPs.
  • Alerts supervisor of processing flow issues.
  • Provides support for casing, staging, quarantine, and QA release of all products.
  • Facilitates donor flow throughout the plasma collection center with a sense of urgency, minimizing wait time by working carefully and efficiently while reallocating personnel as necessary.
  • Alerts management of donor flow issues.
  • Explains plasma collection center policies & rules, educates new donors on the use of therapeutic products made from plasma, donation process, tests performed, proper nutrition, donor fee structure, bonuses, center promotions, and any other information pertinent to the donor.
  • Maintains alertness for donor reactions and assists with reaction and notifies appropriate Medical Staff as needed.
  • Monitors freezer and refrigerator temperatures and immediately informs appropriate personnel if equipment is not functioning properly.
  • Performs quality control on various laboratory equipment (e.g., freezer/refrigerator temperatures, Refractometer, HCT, PCS2 Machines, weight scales or other equipment).
  • Manages product packing, and inventory within freezers for maximum efficiency.
  • Controls disposition of unsuitable product with concurrent documentation.
  • Assists in monitoring inventory levels including stockroom and opening and closing of lots for usage.
  • Receives inventory and maintains storage area for incoming supplies.
  • Prepares product shipment and verification.
  • Classifies and documents the product according to donor programs.
  • Tracks and records data for plasma Specialty Programs, as needed.
  • Reviews donor record files to ensure completeness, accuracy, and compliance with cGMP.
  • Communicates with management regarding pertinent information on work areas and continuous improvement opportunities, as needed.
  • Provides high level of customer service and strives to meet all production goals.
  • Ensures all donor questions are answered timely, accurately, and professionally.
  • Maintains a clean, orderly, and efficient work environment and ensures sufficient operating supplies are available as needed.
  • Follows all SOPs and regulatory policies and procedures, including the employee handbook.
  • Responsible for remaining current on SOPs changes.
  • Follows all Health Safety & Environmental and Occupational Safety and Health Administration (OSHA) policies and procedures.
  • Maintains data integrity and confidentiality of all personnel, donor, and plasma collection center information.
  • Answers the telephone in a courteous manner and provides information or transfer calls to appropriate personnel, as required.

 

 

Education, Qualifications & Experience

  • High school diploma, or equivalent, required.
  • Minimum of one-year experience in a laboratory or warehouse environment preferred.

Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.