Production Technician

U469 (FCRS = US469) AAA USA Inc.; Indianapolis (IN); On-site; USD 35,000 - 64,000; Full time

Benefits offered by this job

Health benefits

401(k) retirement plan

Paid time off

Job summary

Novartis is seeking a Production Technician to support isotope product manufacturing in a controlled environment. You will work with batch records and SOPs, operating Grade C isolators and maintaining safety and compliance throughout production.

Role requires 2+ years in GMP/aseptic pharma settings, ability to handle radioactive materials safely, and strict adherence to procedures. Onsite shift-based work in Indianapolis, with comprehensive US benefits.

Qualifications

• High school diploma or equivalent required; Bachelor's degree strongly preferred.
• Minimum 2 years in GMP or aseptic manufacturing environment.
• Minimum 2 years of pharmaceutical manufacturing experience; low-bioburden preferred.
• Knowledge of GMP regulations and regulated manufacturing environments.
• Ability to work safely with radioactive materials in a controlled setting.
• Experience following SOPs, batch records, and manufacturing documentation.
• Wear cleanroom garments and required respiratory protection.
• Strong attention to detail, communication, safety, quality and compliance.

Responsibilities

• Execute manufacturing activities for isotope products per batch records and procedures.
• Operate and maintain Grade C isolators supporting safe production.
• Follow radiation safety requirements including dosimetry and ALARA.
• Perform contamination control, personnel and material monitoring.
• Support production readiness through cleaning, sterilization and prep.
• Conduct environmental monitoring to maintain readiness and compliance.
• Prepare, verify and maintain materials per batch procedures.
• Participate in qualification and validation activities.
• Complete production documentation including batch records and shipping docs.
• Support safety culture and GMP compliance within the team.

Skills

Attention to detail

Communication

Safety compliance

Education

Bachelor's degree in a scientific discipline

High school diploma or equivalent

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

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.

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.

Salary Range $52,400.00 - $97,400.00

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

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.