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Production Technician (Days)

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About the employer

NovartisPosted on the employer’s careers page · novartis.wd3.myworkdayjobs.comH-1B sponsor: 9 approvals in FY2025–FY2026 — employer-level; what this means

Working in United States

Possible country route: H-1B / other employer-petition routes. H-1B normally starts with an employer petition for a qualifying specialty occupation. Cap-subject cases also have registration and selection requirements; other routes differ.

Registration, petition and consular stages differ. Selection is not guaranteed and premium petition processing is not an end-to-end visa timeline.

What to check before applying
  1. Confirm the intended route. Ask whether the employer will petition and whether the position is cap-exempt.
  2. Check petition requirements. Use USCIS instructions for the applicable category and cap process.
  3. Coordinate consular and entry steps. An approved petition and a work-authorised start date are different milestones.
Official immigration guidance ↗

Reviewed 2026-10-14. Country routes are context, not a confirmation that this vacancy or your passport qualifies.


Description (EN)

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 Days (A Shift)


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.

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. 

To learn more about the culture, rewards and benefits we offer our people click here


 


 

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 us.reasonableaccommodations@novartis.com or call +1(877)395-2339 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
Indianapolis, United StatesOpen in maps ↗

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