Radiopharmaceutical Lab Tech – Night Shift & Sign-On Bonus

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

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.