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Production Lead, Isotopes (3rd shift)

Novartis
  • Indianapolis, Indiana
    14 days ago

    Job Description

    Job Description Summary

    Location: Indianapolis, Indiana

    Relocation Support: This role is based in Indianapolis, Indiana. Novartis is unable to offer relocation support: please only apply if accessible.

    Bring your manufacturing expertise to a role where quality, precision, and teamwork directly support the delivery of isotope products. As a Production Lead, Isotopes, you will play a hands-on role in daily manufacturing while helping guide and develop production technicians, maintain production readiness, and ensure activities are completed safely, on time, and in accordance with current Good Manufacturing Practice and radiation safety requirements. You'll work closely with production leadership and cross-functional partners to promote operational excellence, a strong quality culture, and continuous improvement across the manufacturing environment.

    NOTE: This is a 3rd shift role. Hours are expected to be 10 pm – 6 am, Monday – Friday. Shift schedules may change based on business need.

    #LI-Onsite


     

    Job Description

    Key Responsibilities


    ·    Execute manufacturing activities for Radioligand Therapy isotope products while meeting production, quality, and radiation safety requirements.

    ·    Operate and maintain Grade C isolators in accordance with established procedures and applicable safety requirements.

    ·    Support production readiness through equipment preparation, cell cleaning, isolator sterilization, and environmental monitoring.

    ·    Prepare materials while maintaining material identity and following established batch monitoring procedures.

    ·    Complete batch records, shipping documents, training materials, and other required production documentation accurately and compliantly.

    ·    Support qualification and validation activities while promoting current GMP compliance and a speak-up culture.

    ·    Ensure technicians complete required training and support their professional development to foster a strong growth culture.


    Essential Requirements

    ·    Bachelor of Science strongly preferred; without a degree, a minimum of 2 years of experience in a cGMP or aseptic environment may substitute.

    ·    4+ years of experience in pharmaceutical manufacturing, with low bioburden manufacturing experience preferred.

    ·    Strong understanding of manufacturing and validation requirements and activities.

    ·    Knowledge of cGMP regulations and FDA guidance applicable to isotope manufacturing.

    ·    Proficient in MS Office applications.

    ·    Ability to lift or carry up to 35 pounds.

    ·    Ability to wear cleanroom garments, personal protective equipment, and respiratory protection equipment, including PAPR and respirators.

    ·    Ability to maintain required respiratory protection qualifications, including medical clearance, fit testing, and training, and perform manufacturing activities while wearing respiratory protection equipment for extended periods.


    Desirable Requirements

    ·    Experience or training in radiochemistry or radiopharmacy.

     

     

    The salary for this position is expected to range between $41.05 and $76.25 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

    $85,400.00 - $158,600.00


     

    Skills Desired

    Data Analytics

    Numbers & Facts

    LocationIndianapolis, Indiana
    IndustryBiotechnology/Pharmaceuticals
    Company Size10,000 employees or more
    Year Founded1996
    Websitenovartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

    About Company

    Novartis provides healthcare solutions that improve and extend people’s lives. We use science-based innovation to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. Our company is focused on industry-leading divisions with innovation power and global scale: pharmaceuticals, eye care and generic medicines Novartis is headquartered in Basel, Switzerland. Novartis Group companies employ approximately 120,000 associates and its products are available in more than 180 countries around the world.

    Skills

    • Asepsisunmatched
    • Cleanroomunmatched
    • Continuous Improvementunmatched
    • Cross-Functionalunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Drug Manufacturingunmatched
    • Environmental Monitoringunmatched
    • FDA Requirementsunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Leadershipunmatched
    • Lift/Move 35 Poundsunmatched
    • Manufacturingunmatched
    • Manufacturing Requirementsunmatched
    • Procedure Developmentunmatched
    • Production Supportunmatched
    • Radiation Safetyunmatched
    • Requirements Validation/Verificationunmatched
    • Safety Trainingunmatched
    • Sterilizationunmatched
    • Team Playerunmatched
    • Time Managementunmatched
    • User Documentationunmatched

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