Production Technician I (Weekend PM)

Novartis; Indianapolis (IN); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading company is seeking a Production Technician I for weekend shifts in Indianapolis. The role involves operating isolators, maintaining compliance with cGMP standards, and preparing materials for production. Ideal candidates will have a relevant degree or experience in aseptic environments. Join a team dedicated to delivering innovative therapies.

Qualifications

• Bachelor’s degree in Engineering or Science preferred.
• 1+ year experience in cGMP or aseptic environment.

Responsibilities

• Operate and maintain grade A isolators.
• Prepare materials, maintaining batch integrity.
• Ensure compliance with cGMP activities.

Skills

cGMP

Aseptic Techniques

Collaboration

Education

Bachelor’s degree in Engineering or Science

1+ year experience in cGMP or aseptic environment

Job description

Join to apply for the Production Technician I (Weekend PM) role at Novartis

This role is located on-site in Indianapolis, IN. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Summary

Production Technicians play an active role in the daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Technician adheres to regulatory requirements, executes production according to batch records and SOPs, and works within a team and shift schedule. They collaborate closely with the Manager and Lead to ensure safe and timely production.

Key Responsibilities

1. Operate and maintain grade A isolators, focusing on KPI goals and compliance with radiation safety guidelines.
2. Complete required training on SOPs, aseptic techniques, gowning, and safety protocols.
3. Support production readiness, including cleaning and sterilization of equipment, environmental monitoring.
4. Prepare materials, maintaining batch integrity per procedures.
5. Ensure compliance with cGMP activities and participate in qualification/validation activities.
6. Prepare documentation such as batch records, shipping documents, and training materials.

Shift: Week 1: Thurs-Sun, 6:00pm-6:00am; Week 2: Fri-Sun, 6:00pm-6:00am. Overtime may be required.

Essential Requirements

• Bachelor’s degree in Engineering or Science preferred; alternatively, 1+ year experience in cGMP or aseptic environment.
• Knowledge of cGMP and FDA guidance is preferred.
• Ability to gown aseptically and work in a Grade C clean room environment.
• Near vision of 20/20 (corrected lenses permitted).
• Ability to lift up to 35 pounds.
• Radio Pharma experience is a plus.

Languages

• English

For more about Novartis, our culture, benefits, and equal opportunity statement, please visit our website links provided in the original description.