Plasma Processor

Kedrion Biopharma GmbH; Chicago (IL); On-site; USD 35,000 - 50,000; Full time

Benefits offered by this job

Full medical, dental, and vision coverage

Life insurance

Paid time off

Training programs and development opportunities

Employee discounts

Job summary

Kedrion Biopharma GmbH is hiring a Processing Technician in Chicago, Illinois. In this role, you'll handle crucial steps in plasma processing, emphasizing safety and regulatory compliance. Responsibilities include aseptic procedures, monitoring temperatures, and ensuring product quality. Ideal candidates have a high school diploma, strong attention to detail, and problem-solving skills. The position offers comprehensive benefits including medical coverage and paid time off, fostering career growth and well-being.

Qualifications

• Strong attention to detail and ability to follow strict procedures.
• Ability to work in a fast-paced, regulated environment.
• Familiarity with FDA, cGMP, and OSHA regulations is a plus.

Responsibilities

• Complete aseptic sampling and heat sealing of plasma units.
• Monitor and report freezer temperatures.
• Maintain product safety during processing and storage.

Skills

Attention to detail

Problem-solving skills

Organizational skills

Education

High school diploma or equivalent

Job description

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.

Job Summary

Start your career today! Want to be part of the process that turns plasma donations into life‑saving therapies? As a Processing Technician, you’ll handle the critical steps of plasma processing, sampling, and storage while maintaining compliance with all safety and regulatory standards. Your attention to detail will directly impact the quality of products that help patients around the world.

What you’ll do

• Complete aseptic sampling and heat sealing of plasma units, placing them in freezers within required timeframes to ensure quality.
• Monitor freezer and refrigerator temperatures, reporting any deviations immediately.
• Process plasma and samples according to cGMP, SOPs, and regulatory guidelines.
• Maintain product safety and integrity during processing, storage, and shipment.
• Perform centrifugation, labeling, inspection, and classification of products.
• Prepare, calibrate, and verify equipment maintenance as scheduled.
• Manage product packing, inventory, and freezer organization for efficiency.
• Control the disposition of unsuitable products with complete documentation.
• Prepare and verify shipments according to SOPs.
• Receive and inventory incoming supplies, maintaining a clean and organized storage area.
• Identify released units daily and stage them for shipment.
• Maintain accurate records and data integrity in all processing activities.
• Follow unidirectional flow procedures to prevent cross‑contamination.
• Keep the processing area clean, orderly, and stocked with necessary supplies.
• Answer calls professionally, providing accurate information or transferring to the appropriate person.
• Support production goals while ensuring donor questions are answered clearly and professionally.

Qualifications and need-to-know

• High school diploma or equivalent required.
• Strong attention to detail and ability to follow strict procedures.
• Ability to work efficiently in a fast‑paced, regulated environment.
• Good organizational and problem‑solving skills.
• Willingness to work flexible hours, including evenings, weekends, and holidays as needed.
• Familiarity with FDA, cGMP, and OSHA regulations is a plus.

Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.

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 [e-mail].

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!

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.