Nuclear Manufacturing Technician II - 2nd shift

Cardinal Health•Indianapolis, IN

10d

About The Position

Cardinal Health’s Nuclear Manufacturing team produces time-sensitive radiopharmaceuticals in an integrity-driven, highly regulated environment governed by requirements such as FDA, NRC, and DOT regulations. These products support patient treatment through disease diagnosis, staging, and monitoring. The role manufactures radioactive isotopes and drug products and contributes to production quality, safety, and controlled-area upkeep. This is a full-time second-shift position, Monday through Friday, 3:00 p.m. to 11:30 p.m. Training takes place on the first-shift schedule. The employee must be flexible to work other hours and days, overtime, weekends, and holidays as needed. The position involves routine assignments under a moderate degree of supervision, following standard operating procedures and quality guidelines, and referring complex or unusual problems to a supervisor.

Requirements

High school diploma, GED, equivalent, or equivalent work experience (preferred).
Able to manage weight up to 50 pounds.
Able to work effectively as a team member.
Able to repeatedly follow detailed processing instructions.
Able to multitask and remain well-organized and detail-oriented.
Flexible to work various shifts and schedules as needed.
Comfortable working in a nuclear environment.

Nice To Haves

1–2 years of experience.
Prior manufacturing experience, preferably in a controlled environment and/or regulated industry.
Formulation or aseptic manufacturing experience.
High school diploma, GED, equivalent, or equivalent work experience.

Responsibilities

Manufacture radioactive isotopes and drug products, including synthesis setup, hot-cell manipulations, inspection, packaging, and distribution.
Assemble sterile vials in a controlled environment.
Perform environmental and personnel monitoring.
Maintain strong documentation practices.
Perform clerical and administrative tasks, including maintaining daily production records, preparing reports, and maintaining records.
Manage inventory, including goods receiving, material inspection, and cycle counts.
Perform daily radiation safety tasks and controlled-area cleaning.
Execute Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMP), including Good Documentation Practices (GDP).
Maintain appropriate licenses, training, and certifications.
Follow quality guidelines and refer complex or unusual problems to a supervisor.