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. 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. Employee Benefits 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! Salary ranges are determined based on relevant experience, education, and certifications. 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. Kedrion Biopharma Inc. participates in E‑Verify and provides the federal government with Form I‑9 information to confirm employment authorization. #J-18808-Ljbffr Kedrion Biopharma Inc.