Nuclear Manufacturing Technician II - 2nd shift

Cardinal Health•Indianapolis, IN

11d

About The Position

Nuclear Manufacturing Technician II manufactures time-sensitive radiopharmaceuticals in an integrity-driven, highly regulated environment to support patient treatment through disease diagnosis, staging, and monitoring. The role produces radioactive isotopes and drug products, including synthesis setup, hot cell manipulations, inspection, packaging, and distribution. It also supports sterile assembly, environmental and personnel monitoring, documentation, inventory management, radiation safety, and controlled-area cleaning. Work is performed in accordance with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), and Good Documentation Practices (GDP). This is a full-time second-shift position, Monday through Friday, 3:00 p.m. to 11:30 p.m. Training is completed on a first-shift schedule. The technician must be flexible to work other hours and days, including overtime, weekends, and holidays. The role typically involves routine assignments under a moderate degree of supervision, with regular review of output by a work lead or supervisor; complex or unusual problems are referred to a supervisor.

Requirements

Ability to manage weight up to 50 pounds.
Ability to be an effective team member.
Ability to repeatedly follow detailed processing instructions.
Ability to multitask and remain well-organized and detail-oriented.
Flexibility to work various shifts and schedules as needed, including overtime, weekends, and holidays.
Comfort working in a nuclear environment.

Nice To Haves

1–2 years of experience.
High school diploma, GED, equivalent, or equivalent work experience.
Prior manufacturing experience, preferably in a controlled environment and/or regulated industry.
Formulation or aseptic manufacturing 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) requirements, including Good Documentation Practices (GDP).
Apply acquired knowledge and skills to complete standard tasks, learn and apply new information and methods, maintain appropriate licenses, training, and certifications, and adhere to quality guidelines.
Refer complex or unusual problems to a supervisor.