Nuclear Manufacturing Technician II - 2nd shift

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 myFlexPay

• Flexible spending accounts (FSAs)

• Short- and long-term disability coverage

• Work-Life resources

• Paid parental leave

• Healthy lifestyle programs

Application window anticipated to close: 7/11/2026* if interested in opportunity, please submit application as soon as possible.

What Nuclear Manufacturing contributes to Cardinal Health

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.

Shift/Schedule

• 40 hours weekly / Full Time

• 2nd shift hours

• Monday – Friday 3:00 pm – 11:30 pm

• Must be flexible to work other hours, days, and overtime as needed

Responsibilities

• Manufactures radioactive isotopes and drug products (includes synthesis set up, hot cell manipulations, inspection, packaging, distribution)

• Assemble sterile vials in a controlled environment

• Performs environmental and personnel monitoring

• Demonstrates strong documentation practices

• Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records

• Manages inventory (includes goods receiving, material inspection, and cycle counts)

• Performs daily radiation safety tasks, along with controlled area cleaning

• Execute Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMP) requirements including Good Documentation Practices (GDP)

Qualifications

• 1-2 years of experience, preferred

• High School diploma, GED or equivalent, or equivalent work experience, preferred

• Prior experience in manufacturing, preferably in a controlled environment and/or regulated industry preferred

• Formulation or Aseptic Manufacturing experience preferred

• Ability to manage weight up to 50 pounds

• Ability to be an effective team member.

• Able to repeatedly follow detailed processing instructions

• Multi-task, well-organized and detail-oriented

• formulation or filling experience preferred.

What is expected of you and others at this level

• Applies acquired knowledge and skills to complete standard tasks

• Readily learns and applies new information and methods to work in assigned area

• Maintains appropriate licenses, training and certifications

• Works on routine assignments that require some problem resolution

• Works within clearly defined standard operating procedures and/or scientific methods

• Adheres to all quality guidelines

• Works under moderate degree of supervision

• Work typically involves regular review of output by work lead or supervisor

• Refers complex unusual problems to supervisor