Location: Indianapolis

Job Summary

RayzeBio, a Bristol Myers Squibb company, is seeking applicants for an Environmental Monitoring Technician, I. Reporting to the Assistant Manager of Microbiology, the Environmental Monitoring Technician, I will help support the contamination control and sterility assurance activities for the controlled environments at the manufacturing facility in Indianapolis. This role will conduct environmental monitoring of aseptically produced targeted alpha therapy (TAT) radiopharmaceuticals for RayzeBio’s clinical and commercial programs

Key Responsibilities

• Perform routine environmental monitoring of cleanrooms such as viable airborne monitoring, non-viable particulate sampling, and viable surface monitoring.
• Support aseptic manufacturing activities such as media fills, personnel sampling, etc.
• Ensure the use of proper aseptic techniques and compliance with SOPs during monitoring of controlled environments and utility systems.
• Prepare sample data, results, reports and other documents that are generated from environmental monitoring activities
• General laboratory housekeeping duties and maintenance of the department and equipment.
• Assist in stocking and organizing lab consumables required for environmental monitoring and microbiology testing.
• Read plates to quantify microbial growth and subculture pure isolates as required.
• Support and provide technical, quality, and/or safety information pertaining to environmental monitoring tests to lab management on routine basis.
• Participate in troubleshooting and investigations of environmental excursions to identify root causes and implement corrective actions as required.
• Ensure compliance with GMP regulations, radiation safety guidelines, and quality standards.
• Perform other duties as required by management.
• Generally first shift (6:00 AM-2:30 PM) Monday-Friday, but extended hours or weekend work based on radiopharmaceutical manufacturing schedule may be required.
  
  

Education And Experience

• Associate or bachelor’s degree in biology, Microbiology, or other Life Science related field and 0-1 years of relevant experience in production or quality control in a cGMP/FDA regulated facility.
• A high school diploma may be acceptable with sufficient prior cleanroom and/or environmental monitoring experience in a cGMP/FDA regulated facility
• Experience with sterile manufacturing and/or radiopharmaceuticals preferred.
  
  

Skills & Qualifications

• Work with computer programs, including but not limited to Microsoft Office.
• Highly motivated and organized individual with the ability to work both independently and in a team environment.
• Ability to multi-task and prioritize work based on multiple workflows.
• Strong written and verbal communication skills required.
• Excellent professional ethics, integrity, and ability to maintain confidential information.
  
  

Please click here to apply.