Novartis

Novartis

IT/OT Lab Specialist

Durham

No sponsorshipDetected 73 days ago
PythonProcess ImprovementCustomer SupportRoboticsTest AutomationGMPFDA RegulatoryResearchCommunicationProblem SolvingGxP

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Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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About the role

  • This position will be located in Durham, NC and will be an onsite role.
  • As an IT/OT Lab Specialist at Novartis, you will play a key role in supporting the computerized systems and laboratory technologies that enable scientific innovation and operational excellence.

Responsibilities

  • Support the design, installation, configuration, and maintenance of laboratory instruments, software, and associated hardware.
  • Partner with vendors and internal stakeholders to implement effective system architectures and connectivity solutions.
  • Manage change controls, CAPAs, and system documentation in accordance with GxP requirements.
  • Support FDA inspections, internal audits, and compliance activities across assigned laboratory areas.
  • Drive continuous improvement initiatives that enhance operational efficiency, compliance, and system performance.
  • Strong written and verbal communication skills with the ability to collaborate across diverse teams.
  • We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
  • Automation, Automation Testing, Debugging, Programming Languages, Python (Programming Language), Robotics, Software Testing, Technical Support, Test Automation

Requirements

  • Bachelor's degree in Engineering, Computer Science, Information Technology, or a related technical field.
  • 5+ years of pharmaceutical or biopharmaceutical laboratory operations experience, or equivalent industry experience.
  • Experience installing, configuring, and maintaining laboratory computerized systems in a GMP environment.
  • Experience implementing computerized systems within a corporate network infrastructure.
  • Knowledge of FDA regulations, including 21 CFR Part 11, and other applicable GMP requirements.
  • Experience managing vendor relationships and supporting third-party service providers.
  • Proven troubleshooting and problem-solving abilities in complex, regulated operational environments.
  • Experience with Quality by Design, Six Sigma, or Operational Excellence methodologies.
  • Experience supporting investigations, non-conformances, and computerized system compliance activities.

Skills

  • Job Description Summary

Compensation

  • The salary for this position is expected to range between $98,700 and $183,300 annually
  • 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.
  • $98,700.00 - $183,300.00

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.

Equal opportunity

  • The Novartis Group of Companies are Equal Opportunity Employers.
  • The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities.
  • EEO Statement:
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This listing is sourced directly from Novartis's careers page and normalized into a canonical job model.