Production Technician

Novartis AG; Indianapolis (IN); On-site; USD 35,000 - 64,000; Full time

Job summary

Novartis AG in Indianapolis, IN is seeking a Production Technician to support isotope product manufacturing and radiochemical operations. You will work within a controlled environment, following batch records and SOPs to ensure safety, quality, and timely production.

The role requires handling radioactive materials, operating Grade C isolators, and performing environmental and material monitoring. A science degree and GMP experience are preferred, with a 3rd shift on-site schedule.

Qualifications

• Requires strong GMP/regulatory knowledge.
• Experience handling radiochemical/isotope production environments.
• Familiar with batch records and manufacturing documentation.
• Ability to work in a controlled environment and follow SOPs.

Responsibilities

• Execute manufacturing activities for isotope products per batch records.
• Operate and maintain Grade C isolators in production.
• Follow radiation safety requirements and ALARA principles.
• Perform contamination control and personnel/material monitoring.
• Prepare manufacturing areas and equipment for production readiness.
• Complete production documentation including batch records and shipping docs.
• Support safety, quality, and GMP compliance within the team.

Skills

GMP compliance

Radiation safety

Batch records

Aseptic manufacturing

Equipment operation

Education

Bachelor's degree in science

Tools

Grade C isolators

Environmental monitoring tools

Job description

Job Description Summary

As a Production Technician, you will play an active role in the daily production of isotopes used in advanced radioligand therapies while supporting the setup, preparation, and operation of equipment and manufacturing systems. Working as a qualified radiation worker in a controlled manufacturing environment, you will execute production activities in accordance with batch records, standard operating procedures, and regulatory requirements. Partnering closely with Production Leads and Managers, you will help ensure manufacturing operations are performed safely, efficiently, and on schedule while contributing to therapies that help transform outcomes for patients.

Job Description

#LI-Onsite

Shift: Monday - Friday 3rd Shift

NOTE: This is a 3rd shift role. Hours are expected to be 10 pm - 6 am, Monday - Friday. Shift schedules may change based on business need.

Location: Indianapolis, IN, United States

Relocation Support : This role is based in Indianapolis, IN, United States. Novartis is unable to offer relocation support: please only apply if accessible.

Key Responsibilities

• Execute manufacturing activities for isotope products in accordance with batch records and established procedures.
• Operate and maintain Grade C isolators while supporting safe, compliant production operations.
• Follow radiation safety requirements, including dosimetry, personal protective equipment, and ALARA principles.
• Perform contamination control, personnel monitoring, and material monitoring in accordance with site procedures.
• Support production readiness through equipment cleaning, sterilization, and preparation of manufacturing areas.
• Conduct routine and dynamic environmental monitoring to maintain manufacturing readiness and compliance.
• Prepare, verify, and maintain materials in accordance with defined batch monitoring procedures.
• Participate in qualification and validation activities to support operational readiness and process compliance.
• Complete production documentation, including batch records, shipping documents, and training records.
• Support a culture of safety, quality, current Good Manufacturing Practice compliance, and open communication within the manufacturing team.

Essential Requirements

• High school diploma or equivalent required; Bachelor's degree in a scientific discipline strongly preferred.
• Minimum 2 years of experience in a current Good Manufacturing Practice or aseptic manufacturing environment.
• Minimum 2 years of pharmaceutical manufacturing experience; low-bioburden manufacturing experience preferred.
• Knowledge of current Good Manufacturing Practice regulations and regulated manufacturing environments.
• Ability to work safely with radioactive materials in a controlled manufacturing environment.
• Experience following standard operating procedures, batch records, and manufacturing documentation.
• Ability to wear cleanroom garments, personal protective equipment, and required respiratory protection.
• Strong attention to detail, communication skills, and commitment to safety, quality, and compliance.

Desirable Requirements

• Training in radiochemistry or radiopharmacy strongly preferred.
• Hands‑on experience in radiochemistry, isotope production, or radiopharmaceutical manufacturing with radioactive materials in a Good Manufacturing Practice environment strongly preferred.

Languages

English

Salary

The salary for this position is expected to range between $25.19 and $46.82 per hour. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance‑based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US‑based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Salaries are also indicated at a yearly level: $52,400.00 - $97,400.00.

EEO Statement

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.

Accessibility and reasonable accommodations

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 [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired

Forklift Operations, GMP Compliance, Health, Safety and Environment (HSE) Policy, Inventory Management, Machine Operations, Manufacturing, Operations Management, Process Improvements, Production Management, Quality Control (QC), Regulatory Documents