Production Technician I (Weekday PM)
Indianapolis, IN - USA
Job Summary
Job Description Summary
Join 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.
Job Description
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 materialsmaintainidentity and traceability and update the batch monitoring system as.
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:
Bachelors 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 is.
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 healthlifeand disability benefits a 401(k) with company contribution and match and a variety of other addition employees are eligible for a generous time off package including vacation personal daysholidaysand 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 or call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Salary Range
$52400.00 - $97400.00Skills 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 SchedulerRequired Experience:
IC
About Company
Novartis is a global healthcare company based in Switzerland that provides solutions to the evolving needs of patients worldwide.