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Production Support Manager

Novartis
  • Indianapolis, Indiana
    3 days ago

    Job Description

    Band

    Level 4


     

    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.

    Take the next step in your Novartis career and help strengthen production performance at our Indianapolis site. As Production Support Manager, you will lead the Process Expert Support team and play a key role in enabling reliable, compliant, on-time and cost-effective production delivery. You will provide leadership across deviation investigations, corrective and preventive actions, change controls, production documentation, training, and continuous improvement initiatives while partnering closely across functions to resolve complex challenges and improve performance. This is an opportunity to expand your leadership impact, develop team capabilities, and help advance a culture of safety, quality, inclusion, and continuous improvement.

    #LI-Onsite


     

    Job Description

    Key Responsibilities

    ·    Lead and develop the Process Expert Support team to effectively support production operations.  

    ·    Ensure certified deviation investigators and change control owners are available to meet current site demand.

    ·    Oversee training of the production support team, including investigators, subject matter experts, and cross-functional support resources.

    ·    Track deviations, corrective and preventive actions, and change controls to ensure timely closure and key deliverables.

    ·    Review, approve and own production investigations, support risk assessments and root-cause analysis, and assign actions to prevent recurrence.

    ·    Review documentation to support manufacturing, including Standard Operating Procedures, batch records, white papers, validation documents, work orders, etc.

    ·    Drive process optimization, manufacturing workflow improvements, new technology introduction, and site-wide continuous improvement initiatives.


    Essential Requirements

    ·    Bachelor's degree in engineering, science, or a related field, or equivalent experience.

    ·    5+ years of experience in manufacturing, quality, or a related technical field within the pharmaceutical industry.

    ·    Prior leadership experience.

    ·    Strong communication, analytical, and problem-solving skills.

    ·    Demonstrated history of working collaboratively across functions and sites, with change management skills, adaptability, and ability to work under pressure.

    ·    Knowledge of cGMP requirements and continuous improvement within a regulated environment; ability to travel approximately 5%.


    Desirable Requirements

    ·    Radiopharmaceutical experience.

     

     

    The salary for this position is expected to range between $108,500 - $201,500 per year. 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, 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

    $108,500.00 - $201,500.00


     

    Skills Desired

    Data Analytics, Digital Literacy, Health, Safety, and Environment (HSE) Policy

    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

    • Analysis Skillsunmatched
    • Biotech and Pharmaceuticalunmatched
    • Change Controlunmatched
    • Change Managementunmatched
    • Communication Skillsunmatched
    • Continuous Improvementunmatched
    • Corrective Actionunmatched
    • Cross-Functionalunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Customer Service Managementunmatched
    • Document Managementunmatched
    • Documentation Reviewunmatched
    • Leadershipunmatched
    • Manufacturingunmatched
    • Operational Supportunmatched
    • Performance Managementunmatched
    • Problem Solving Skillsunmatched
    • Process Developmentunmatched
    • Process Improvementunmatched
    • Process Manufacturingunmatched
    • Production Controlunmatched
    • Production Costingunmatched
    • Production Supportunmatched
    • Risk Analysisunmatched
    • Root Cause Analysisunmatched
    • Safety/Work Safetyunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Support Documentationunmatched
    • Time Managementunmatched
    • Validation Documentationunmatched
    • White Papersunmatched
    • Willing to Travelunmatched

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