Novartis
radioligand therapy manufacturing
ProductionTechnician(weekenddays)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Production Technician (weekend days) at Novartis. Skills: radioligand therapy manufacturing, aseptic techniques, advanced manufacturing systems, regulatory compliance, current Good Manufacturing Practice. Manufacture radioligand therapy products by following batch instructions and maintaining strict aseptic discipline. Operate and maintain Grade A isolators to meet safety, quality, and key performance indicator targets”
What You'll Achieve.
ensuring every product is manufactured safely, accurately, and on time; meet safety, quality, and key performance indicator targets
Industry & Context.
Ability to lift or carry up to 35 pounds, perform hands-on production tasks, Near vision equivalent to 20/20 with no color vision corrective lenses permitted
What They're Looking For.
Must Have
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 to gown aseptically and work extended periods in a Grade C cleanroom environment, attention to detail and ability to complete batch records and controlled documentation accurately, Near vision equivalent to 20/20 with no color vision corrective lenses permitted, Ability to lift or carry up to 35 pounds and perform hands-on production tasks
Nice to Have
Radiopharmaceutical manufacturing experience preferred, especially in aseptic or cleanroom operations, English proficiency for reading, writing, and speaking in a regulated manufacturing environment
What You'll Do.
Manufacture radioligand therapy products by following batch instructions and maintaining strict aseptic discipline
Operate and maintain Grade A isolators to meet safety
and key performance indicator targets
Follow radiation safety requirements and comply with all state
and Novartis guidelines
Complete required training in Standard Operating Procedures
gowning qualification
Clean production cells manually and sterilize isolators to ensure production readiness
Perform routine and dynamic environmental monitoring per procedure and document results accurately
maintain identity and traceability
and update the batch monitoring system as required
Execute work in alignment with current Good Manufacturing Practice and site quality standards
Support qualification and validation contribute to deviation investigations and inspection readiness
Prepare and maintain batch records
shipping documentation
and training materials to ensure compliant operations
How You'll Work.
Team & Collaboration
Reliable teamwork and communication skills to succeed in a fast-paced, shift-based schedule
Communication Scope
communication skills
Full Job Description
**Job Description Summary** #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. 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: Thursday–Sunday one week, Friday–Sunday the following week, 6:00 a.m.–6:00 p.m.; mandatory overtime may be required **Job Description** **Key Responsibilities:** · Manufacture radioligand therapy products by following batch instructions and maintaining strict aseptic discipline. · Operate and maintain Grade A isolators to meet safety, quality, and key performance indicator targets. · Follow radiation safety requirements and comply with all 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 ensure production readiness. · Perform routine and dynamic environmental monitoring per procedure and document results accurately. · Prepare materials, maintain identity and traceability, and update the batch monitoring system as required. · Execute work in alignment with current Good Manufacturing Practice and site quality standards. · Support qualification and validation
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