X Production Technician, Weekend

2 X Production Technician, Weekend Days – Novartis

Location:

Indianapolis, IN. This position is located on site; relocation support is not available.

Shift: Weekend Day Shift. This role may involve mandatory overtime as needed.

Job Overview

Production Technicians play an active role in the daily production of Radioligand Therapies (RLT) and in the setup and preparation of instruments and equipment. The Technician ensures compliance with regulatory requirements while executing production per batch records and SOPs, working within a team and according to the shift schedule. The Technician closely collaborates with the Manager and Lead to ensure safe and timely production.

• Execute all activities related to the manufacturing of RLT products. Responsibilities include operating and maintaining Grade A isolators, focusing on KPI goals and ensuring compliance with state, federal and Novartis radiation safety guidelines.
• Successfully complete required training curriculum comprising SOPs, Aseptic Techniques, Gowning Qualifications, and other relevant training including HSE for the specific role, within the assigned time.
• Support all technical aspects related to production readiness, including manually cleaning the cell and performing sterilization of isolators and conducting routine and dynamic environmental monitoring as required.
• Prepare all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
• Ensure all cGMP compliance activities are followed.
• Participate in assigned qualification/validation activities, and assist on deviation investigations and inspections as necessary.
• Prepare 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’s 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 should be equivalent to 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.
• 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 or call  and let us know the nature of your request and your contact information.

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