Lab Technician

Cardinal Health; New Orleans (LA); Sur place; USD 42 000 - 46 000; Plein temps

Avantages offerts par ce poste

Medical, dental and vision coverage

Paid time off

Health savings account (HSA)

401k savings plan

Access to wages before pay day with my

Résumé du poste

Cardinal Health is seeking personnel for Nuclear Manufacturing in New Orleans to manufacture PET radiopharmaceuticals and support patient diagnosis through regulated production processes.

The role involves extensive training, ISO cleanroom work, and strict adherence to cGMP/GDP. You will handle radioactive materials, perform QC tests, and collaborate with cross-functional teams in a fast-paced environment.

Qualifications

• Must be able to work overnight shift (Facility operates at night).
• Prior manufacturing experience in a controlled/regulatory environment preferred.
• Strong written and spoken English communication skills required.

Responsabilités

• Complete extensive training and hands-on components to demonstrate proficiency.
• Manufacture radioactive isotopes and conduct quality control testing on batches.
• Work in ISO cleanrooms to prepare product and customer vials.
• Perform environmental and personnel monitoring across ISO levels.
• Coordinate daily production run schedules based on customer needs.
• Maintain daily production records and SOP-compliant documentation.
• Manage SAP Inventory including receiving and cycle counts.
• Execute cGMP and GDP compliant procedures and maintain sterile environments.
• Collaborate with cross-functional teams to meet production goals.

Connaissances

Overnight shift ability

English communication

Team player

Manual dexterity

Ability to lift 50-75 lbs

Quality and safety awareness

Formation

High school diploma/GED

Science education preferred

Outils

SAP Inventory

Description du poste

Sign on Bonus: $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 40 hours per week. The typical schedule is Monday through Friday with a start time anywhere between the hours of 9:00p and 1:00a. ( 8 hour shift). Also, working a Saturday and Sunday once a month. Candidate must be flexible to work different days, hours and schedules based on business need.

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


• 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

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.

Bonus eligible

No Pay Rate: $20.00 per hour to start and then after 6 months completion of certification pay will increase to $22.00 per hour.

Benefits

• 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

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.

Headquartered in Dublin, Ohio, Cardinal Health, Inc. (NYSE: CAH) is a distributor of pharmaceuticals, a global manufacturer and distributor of medical and laboratory products, and a provider of performance and data solutions for healthcare facilities. We are a crucial link between the clinical and operational sides of healthcare, delivering end‑to‑end solutions and data‑driving insights that advance healthcare and improve lives every day. With deep partnerships, diverse perspectives and innovative digital solutions, we build connections across the continuum of care. With more than 50 years of experience, we seize the opportunity to address healthcare's most complicated challenges — now, and in the future.

To read and review this privacy notice click here