Nuclear Manufacturing Technician II - Day shift

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
• Monday – Friday 7:00 am – 3:30 pm
• Must be flexible to work other hours and days as needed including weekends and holidays

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
• Flexibility to work various shifts/schedules as needed
• Comfortable working in a nuclear environment

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

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

To read and review this privacy notice click here