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.

QUALIFICATIONS:

• Bachelor’s degree in Microbiology or Biological Sciences.
• Previous experience with microbiological and environmental monitoring techniques is preferred.
• Prior experience with aseptic techniques is preferred.
• Experience in a Quality Control or cGMP environment is a plus.
• Strong written and verbal communication skills.
• Excellent organizational skills and proficiency with Microsoft Office Suite.
  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

You’ll perform general and moderately technical microbiological duties, including testing in-process samples, raw materials, finished products, and stability samples. Your responsibilities also include extensive environmental monitoring (EM) and meticulous documentation.

Key Responsibilities include:

• Microbiological Testing: Execute techniques for in-process samples and raw materials, including Microbial Support Testing (NAT, Growth Promotion), EM Water Testing, and Microbial Testing for Bioburden and LAL.
• Environmental Monitoring (EM): Conduct EM for facilities, utilities (Pharm Air, Nitrogen), and laboratories. This includes viable air, contact plates, passive air, and total particulate counts.
• Laboratory Support: Assist with essential lab management tasks such as housekeeping, equipment calibration, safety inspections, and shipping samples.
• Documentation: Maintain accurate records by reviewing logbooks, initiating lab investigations and deviations, and entering data for trending. You will also review SOPs and ensure all training is up to date.