QC Technician
About The Position
Help reimagine cancer care by shaping how our Radioligand Therapies (RLT) reach more patients—safely, reliably, and faster. At Novartis, we’re pioneering the future of treatment through the fusion of nuclear medicine and precision oncology We are seeking a highly motivated and detail-oriented Quality Control (QC) Technician to support Chemistry functions at our radioisotope production site. The primary responsibility of this role will be to perform routine quality control testing and analytical functions to ensure the production of high-quality radioisotopes. The QC Technician will work closely with the Quality Control and Production teams to maintain regulatory compliance, meet GMP (Good Manufacturing Practices) standards, and ensure the safety and efficacy of products produced at our Indianapolis Isotopes facility. Location: Indianapolis, IN #LI-Onsite Shift: This position involves off - shift and weekend work which will be defined through site start up and commercialization readiness. This role is located on-site in Indianapolis, IN. Novartis is unable to offer relocation support for this role; please only apply if this location is accessible for you.
Requirements
- Bachelor’s degree in chemistry or a related field.
- A minimum of 2 years of experience in a laboratory or quality control environment, preferably in the pharmaceutical, biotechnology, or radiopharmaceutical industry.
- Experience with chemical testing techniques is required.
Nice To Haves
- Experience with Quality Control laboratory instrumentation and equipment is highly desirable.
Responsibilities
- Perform routine testing on raw materials and finished products.
- Perform routine chemical testing, including ICP (Inductive Couple Plasma), TLC (Thin Layer Chromatography), Gamma Spectroscopy and pH testing, to assess the chemical quality of products.
- Perform routine testing on raw materials, in-process samples, and finished products.
- Maintain and calibrate laboratory equipment and instruments.
- Ensure proper sampling and testing of raw materials, in-process materials, and final products in compliance with established protocols and specifications.
- Assist in the validation and qualification of analytical methods for the testing of Lutetium Chloride and other radioisotope-related products.
- Maintain accurate records of all laboratory activities in compliance with GMP and regulatory requirements.
Benefits
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
