
Band
Level 2Join a team at the forefront of radioligand therapy manufacturing and play a vital role in delivering innovative treatments to patients who need them most. As a Production Technician I, you will be hands-on in a highly controlled, cutting-edge environment, ensuring every product is manufactured safely, accurately, and on time. This is an opportunity to build your expertise in aseptic techniques, advanced manufacturing systems, and regulatory compliance, while contributing directly to life-changing therapies. If you are energized by fast-paced production environments and take pride in precision, quality, and teamwork, this role offers the chance to make a meaningful impact every day.
Shift: Monday-Thursday 6pm-6am and then Monday-Wednesday 6pm-6am
#LI-Onsite
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:
Manufacture radioligand therapy products by following batch instructions andmaintainingstrict aseptic discipline.
Operate andmaintainGrade A isolators to meet safety, quality, and key performance indicator targets.
Follow radiation safety requirements andcomply withall state, federal, and Novartis guidelines.
Complete required training in Standard Operating Procedures, aseptic technique, gowning qualification, and Health, Safety, and Environment.
Clean production cells manually and sterilize isolators to ensureproductionreadiness.
Perform routine and dynamic environmental monitoring per procedure and document results accurately.
Prepare materials,maintainidentity and traceability, and update the batch monitoring system asrequired
Execute work in alignment with current Good Manufacturing Practice and site quality standards.
Support qualification and validation activities; contribute to deviation investigations and inspection readiness.
Prepare andmaintainbatch records, shipping documentation, and training materials to ensure compliant operations.
Essential Requirements:
Bachelor’s degree in relevant Engineering or Scientific discipline is highly preferred; If the applicant does not have a degree, a minimum of 1+ year’ of experience in cGMP or aseptic environment isrequired
Working knowledge of current Good Manufacturing Practice for sterile or aseptic manufacturing environments.
Ability to follow United States Food and Drug Administration guidance relevant to aseptic manufacturing.
Ability togownaseptically and work extended periods in a Grade C cleanroom environment.
Strong attention to detail and ability to complete batch records and controlled documentation accurately.
Near vision equivalent to 20/20 with no color vision impairment; corrective lensespermitted
Ability to lift or carry up to 35 pounds and perform hands-on production tasks.
Reliable teamwork and communication skills to succeed in a fast-paced, shift-based schedule.
Desirable Requirements:
Radiopharmaceutical manufacturing experience preferred, especially in aseptic or cleanroom operations.
Englishproficiencyfor reading, writing, and speaking in a regulated manufacturing environment.
NovartisCompensation and Benefits:
The salary for this position is expected to range between $25.19/hr. and $46.83/hr.
The final salary offered isdeterminedbased 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,lifeand 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,holidaysand 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, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
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 in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com 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.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings
Salary Range
$52,400.00 - $97,400.00
Skills Desired
Assembly Language, Cooperation, Efficiency, Electronic Components, Flexibility (Inactive), General Hse Knowledge , Good Documentation Practice, Installations (Computer Programs), Iso (International Organization For Standardization), Job Description, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Nuclear Medicine, Physics, Product Distribution, Production Line, Scheduler

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.
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