Production Technician I (Weekend PM)

Novartis Contract Manufacturing; Indianapolis (IN); On-site; USD 50,000 - 75,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking individuals for a role focused on the production of RLT products. Responsibilities include operating grade A isolators and ensuring compliance with cGMP standards. Candidates with a background in engineering or science, or experiences in aseptic environments, will find this opportunity rewarding. Join an innovative community dedicated to improving patient lives.

Qualifications

• Knowledge of cGMP and FDA guidelines preferred.
• Near vision of 20/20 with no color vision impairment.
• Ability to lift up to 35 pounds.

Responsibilities

• Execute all activities related to the manufacturing of RLT products.
• Prepare and maintain batch records and shipping documents.
• Support production readiness, including cleaning and sterilization.

Skills

Knowledge of cGMP

Aseptic techniques

Ability to gown aseptically

Education

Bachelor’s degree in Engineering or Science

1+ year experience in cGMP or aseptic environment

Job description

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Summary

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.

About The Role

Key Responsibilities:

• Execute all activities related to the manufacturing of RLT products, including operating and maintaining grade A isolators, focusing on KPI goals, and adhering to all radiation safety guidelines.
• Complete required training on SOPs, aseptic techniques, gowning, and safety protocols.
• Support production readiness, including cleaning and sterilization of isolators, and environmental monitoring.
• Prepare materials maintaining proper identification and documentation.
• Ensure compliance with cGMP standards.
• Participate in qualification/validation activities and assist with deviations and inspections.
• Prepare and maintain 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 guidelines preferred.
• Ability to gown aseptically and work in a Grade C clean room environment.
• Near vision of 20/20 with no color vision impairment.
• Ability to lift up to 35 pounds.
• Radio Pharma experience is a plus.

Languages: English

Why Novartis: Join a community dedicated to transforming patient lives through innovation and collaboration. Learn more at Novartis Strategy.

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EEO Statement: We are equal opportunity employers and do not discriminate based on legally protected characteristics.

Accessibility & Reasonable Accommodations: For accommodations, contact [e-mail] or call [phone], including the job requisition number.