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Medical Screener (Cinnaminson, NJ, US, 08077)

Kedrion Biopharma Inc. · Cinnaminson, Vereinigte Staaten Von Amerika · Onsite

  • Professional
  • Optionales Büro in Cinnaminson
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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 [email protected].


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

Job Description

  • Greet and register donors, ensuring accurate and timely data entry.
  • Guide donors through the health screening process, including reviewing self-administered health history forms and determining if further medical review is needed.
  • Perform vital signs assessments (blood pressure, pulse, temperature, weight) and fingerstick blood sampling to measure hematocrit and total protein levels.
  • Prepare and calibrate screening equipment according to SOPs, performing basic troubleshooting as needed.
  • Monitor donor safety during the screening and donation process, identifying and reporting adverse reactions to medical staff.
  • Explain the donation process, plasma center policies, and donor safety guidelines in a clear and professional manner.
  • Maintain accurate donor records and ensure all documentation meets cGMP and regulatory requirements.
  • Operate internal computer systems, including the National Donor Deferral Registry (NDDR) and Cross Donation Check System (CDCS), according to approved guidelines.
  • Maintain a clean, organized, and well-stocked work area, including updating supply lot numbers when new lots are introduced.
  • Support the plasmapheresis process by preparing collection machines, monitoring donor comfort, and assisting with disconnection procedures when needed.
  • Participate in center audits by providing accurate records and compliance documentation.
  • Work collaboratively with other staff to meet production goals and maintain a positive donor experience.
  • Answer donor and public inquiries in a courteous and knowledgeable manner, transferring calls as necessary.

 

Qualifications:

  • High school diploma or equivalent required.
  • At least 1 year of customer service experience, preferably in a healthcare, retail, or plasma/blood collection setting.
  • Clinical Laboratory Personnel license required in the State of Louisiana.
  • Strong interpersonal skills with the ability to communicate clearly and professionally.
  • Detail-oriented with a commitment to accuracy and regulatory compliance.
  • Willingness to work flexible hours, including evenings, weekends, and holidays as needed.
  • Familiarity with FDA, cGMP, and OSHA standards is a plus.

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.