X Production Technician - Night Shift

2 x Production Technician – Night Shift

Location:

Indianapolis, IN (on-site). Novartis is unable to offer relocation support for this role; please only apply if this location is accessible for you.

This role is located on‑site in Indianapolis, IN and requires a commitment to safety and regulatory compliance. The Production Technician plays an active role in daily production of Radioligand Therapies (RLT) and is responsible for the setup and preparation of instruments and equipment.

Week Nights – Monday through Friday, 1:00 pm to 10:00 am. This position may involve mandatory overtime as needed.

Additionally, a 12‑hour rotating shift is offered: 6:00 pm to 6:00 am. This position may involve mandatory overtime as needed.

• Executes all activities related to the manufacturing of RLT products, operating and maintaining Grade A isolators and focusing on KPI goals while adhering to all state, federal and Novartis radiation safety guidelines.
• Responsible for the successful, on‑time completion of required training curriculum comprising the necessary Standard Operating Procedures (SOPs), aseptic techniques, gowning qualifications and other relevant training including HSE for the specific role.
• Supports all technical aspects related to production readiness, including manual cleaning of the cell and performing sterilization of the isolators; conducts routine and dynamic environmental monitoring as required.
• Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
• Ensures all cGMP compliance activities are followed.
• Participates in assigned qualification/validation activities and assists on deviation investigations and inspections, as necessary.
• Prepares applicable documents and records such as batch records, shipping documents and training materials.

• Bachelor’s degree in a relevant engineering or scientific discipline is highly preferred; if the applicant does not have a degree, a minimum of 1+ year of experience in a cGMP or aseptic environment is required.
• Knowledge of cGMP regulations and FDA guidance applicable to aseptic manufacturing is highly preferred.
• Ability to gown aseptically and work in a clean‑room environment (Grade
  
  C) area for extended periods of time is required.
• Near‑vision performance equivalent to 20/20 with no impairment of color vision; corrective lenses may be used to achieve the desired visual acuity.
• Ability to lift or carry up to 35 pounds.
• Radio Pharma experience preferred.

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The Novartis Group of Companies are equal‑opportunity employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please send an e‑mail to us.reasonab or call +1‑877‑395‑2339 and let us know the nature of your request and your contact information.

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Entry level