IT/OT Lab Specialist

NovartisDurham, NC
Onsite

About The Position

Imagine being the technology partner who keeps critical laboratory operations running smoothly, compliantly, and efficiently every day. 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. You'll work alongside cross-functional teams to ensure reliable system performance, maintain compliance with regulatory requirements, and help deliver the technology foundation that supports our mission to reimagine medicine for patients worldwide.

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.
  • Strong written and verbal communication skills with the ability to collaborate across diverse teams.
  • Experience managing vendor relationships and supporting third-party service providers.
  • Proven troubleshooting and problem-solving abilities in complex, regulated operational environments.

Nice To Haves

  • Experience with Quality by Design, Six Sigma, or Operational Excellence methodologies.
  • Experience supporting investigations, non-conformances, and computerized system compliance activities.

Responsibilities

  • Support the design, installation, configuration, and maintenance of laboratory instruments, software, and associated hardware.
  • Ensure high availability and reliable performance of laboratory computerized systems and equipment.
  • Partner with vendors and internal stakeholders to implement effective system architectures and connectivity solutions.
  • Execute maintenance activities, user reviews, audit trail reviews, and other system lifecycle requirements.
  • 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.

Benefits

  • performance-based cash incentive
  • eligibility to be considered for annual equity awards
  • health, life and disability benefits
  • a 401(k) with company contribution and match
  • a variety of other benefits
  • generous time off package including vacation, personal days, holidays and other leaves
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