Sr Production Chemist, Nuclear Manufacturing

Anticipated salary range: $68,500 - $97,800

Bonus eligible: No

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

• Medical, dental and vision coverage
• Paid time off plan
• Health savings account (HSA)
• 401k savings plan
• Access to wages before pay day with myFlex Pay
• Flexible spending accounts (FSAs)
• Short- and long-term disability coverage
• Work-Life resources
• Paid parental leave
• Healthy lifestyle programs

Application window anticipated to close: 11/25/2025
* if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate?s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment.

Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring.

• 40 hours weekly - Full Time
• 2nd shift hours
• Monday - Friday 3:00pm - 11:30pm
• Training will start on 1st shift
• Must be flexible to work other hours and days as needed

• Support the manufacturing activities from internal product development and external sponsors.
• Receive, sample, store and/or distribute all materials required for production.
• Safely receive, handle, and transfer radioactive isotopes and final products to end users.
• Facilitate day-to-day operation and maintenance of the facility, production equipment, radiation monitoring equipment, and testing instrumentation.
• Perform hands‑on execution of manufacturing procedures, following standard operating procedures (SOPs), master batch records (MBRs), and protocols.
• Lead and/or support investigations and documentation of deviations and non‑conformances.
• Clean and maintain all production equipment, including clean rooms and isolators.
• Record and maintain systems regarding cGMP compliance such as consumable inventory levels, area classification requirements, or site environmental monitoring.
• Communicate all issues related to safety, quality, and compliance to site leadership.
• Perform relevant documentation for maintenance activities, as well as modify and/or create SOPs.
• Provide input to the Product Development team regarding client drug manufacturing.

• Bachelor?s degree in life sciences or engineering with at least 2 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology industry.
• Demonstrated familiarity with the operation, use, and cleaning of laboratory scale production equipment.
• Ability to work in a controlled environment requiring special attention to environmental, health, and safety regulation.
• Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements; ability to clearly document all work activities in a timely manner.
• Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.
• Flexibility to work periodic off‑shift hours in support of routine production.
• Experience working in clean rooms/ISO5-8 environments/isolators not required, but is a plus.
• Experience working with radioactive isotopes not required, but is a plus.
• Must be able to lift up to fifty (50) pounds

• Applies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks
• Works on projects of moderate scope and complexity
• Identifies possible solutions to a variety of technical problems and takes action to resolve
• Applies judgment within defined parameters
• Receives general guidance and may receive more detailed instruction on new projects
• Work reviewed for sound…