Senior Engineer, Automation

Novartis

Durham, NC, US
Base: $108,500 to $201,500 annually; bonus/equity:...
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8 years pharmaceutical gmp experience
Dcs bms plc scada programming
S88 methodology application
** Novartis is seeking a Senior Automation Engineer for their Aseptic Drug Product facility in Durham, NC. The role involves leading automation design, ensuring compliance with standards, and supporting the site’s manufacturing operations. **

Job Summary

  • The Senior Automation Engineer will provide technical leadership and design oversight for automation systems within a Novartis Aseptic Drug Product facility in Durham, NC.
  • Candidates must possess extensive experience in pharmaceutical GMP manufacturing operations, including the development of lifecycle documentation and execution of system-level qualification testing.
  • The role offers a competitive salary range between $108,500 and $201,500 annually, along with performance-based cash incentives, equity awards, and comprehensive health benefits.

Matching Summary

Match Score: 75

** Novartis is seeking a Senior Automation Engineer for their Aseptic Drug Product facility in Durham, NC. The role involves leading automation design, ensuring compliance with standards, and supporting the site’s manufacturing operations. **

Salary

Base: $108,500 to $201,500 annually; Bonus/Equity: Performance-based cash incentive and annual equity awards eligibility; Benefits: Health, life, disability, 401(k) match, and generous time off package

Skills & Requirements

Must-have

  • 8 years pharmaceutical GMP experience
  • DCS BMS PLC SCADA programming
  • S88 methodology application
  • 21 CFR Part 11 knowledge
  • System qualification testing execution
  • Change control documentation writing

Nice-to-have

  • Strong project management skills
  • Leadership of small engineering teams
  • Continuous improvement mindset
  • Contractor management experience
  • Rotating on-call availability

Key Requirements

  • B.S. degree in Engineering or Computer Science
  • 8 years work experience in pharmaceutical GMP
  • In-depth knowledge of FDA regulations
  • Experience with field wiring and panel design

Work Rights

Not specified

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