Lab Technician

Sign on Bonus

• Now offering a $1500 new hire sign-on bonus!!

What Nuclear Manufacturing contributes to Cardinal Health

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.

The primary work environment consists of a cyclotron and associated manufacturing facility to produce PET radiopharmaceuticals, which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Employees handle radioactive materials and are exposed to very low amounts of radiation that are deemed safe by current standards. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory group. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he / she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.

Schedule

Bonus eligible : No

Pay rate : $22.50 per hour

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 : 11 / 14 / 2025

Responsibilities in this role Successfully complete extensive training, including e-learning assignments and hands on components, to demonstrate and maintain proficiency

Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution)

Conducts quality control testing of each batch (utilizing gas chromatograph, dose calibrator, multi-channel analyzer, TLC plate scanner, high pressure liquid chromatograph, analytical balance, PTS, laminar flow hood and fume hood)

Works in ISO 7 cleanroom to make product vials and customer vials for use in drug production

Performs environmental and personnel monitoring in ISO 5, ISO 7, and ISO 8 environments

Coordinates daily production run schedule based on customer and pharmacy needs

Demonstrates strong documentation practices, oral communication, and writing skills. Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records

Manages SAP Inventory (includes receiving materials, properly inspecting materials for use, and maintaining proper cycle counts)

Performs daily radiation safety tasks, along with general lab cleaning

Qualifications

High school diploma, GED or equivalent, or equivalent work experience, preferred

Education in sciences preferred

Lab experience highly preferred

Must be able to work overnight shift (Facility operates at night.)

Prior experience in manufacturing, preferably in a controlled environment and / or regulated industry desired.

Effective written and verbal English communication skills required

Able to repeatedly follow detailed processing instructions

Ability to manage several tasks at the same time; Ability to evaluate operating conditions and exercise sound judgment and problem-solving skills.

Lifting : Frequent lifting between 50-75 lbs.

Ability to see fine particulate and differentiate colors in liquid solutions.

Ability to hear, write (English), and speak (English) clearly to communicate in manufacturing setting.

Manual dexterity required for equipment operation and occasional reach and lifting of small objects.

Ability to be an effective team member.

What is expected of you and others at this level in Nuclear Manufacturing for functional success

Ability to execute Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMP) requirements including Good Documentation Practices (GDP)

Ability to monitor and verify quality in accordance with SOPs

Ability to perform general maintenance

Ability to work in and maintain a sterile environment, including required cleaning of equipment and facility

Work in partnership with cross functional teams to ensure product / production expectations and demands are met

Disciplined approach to adhering to a large volume of SOPs, with the ability to adapt to process improvements

Ability to learn and utilize technology to support manufacturing processes

Ability to manage inventory

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

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 / Affirmative Action 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.

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