Senior Automation Engineer – GMP Pharma (CIP/SIP, DeltaV)

Novartis Group Companies

Durham (NC)

Vor Ort

USD 99.000 - 183.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Novartis Group of Companies in Durham, NC is seeking an Automation Engineer III focused on compounding, CIP, SIP and utility distribution to help ensure compliant, reliable pharmaceutical manufacturing.

You will troubleshoot, implement improvements, support validation, and collaborate with Manufacturing and Quality across the site. This onsite role requires a Bachelor's degree and 5+ years GMP experience with DeltaV, OSI PI, PLC/SCADA.

Qualifikationen

  • Bachelor's degree in Engineering, Computer Science, or a related technical field.
  • Minimum 5 years GMP manufacturing experience or 9 years equivalent.
  • Hands-on experience with DCS platforms, preferably DeltaV.

Aufgaben

  • Maintain and optimize compounding, CIP/SIP, and utility automation systems.
  • Design, configure, install, and lifecycle-manage automation hardware and software.
  • Develop control strategies for compounding, CIP, SIP, and utility systems.
  • Lead automation activities for capital projects and system upgrades.
  • Create URS, FS, DDS, HDS, and SDS documentation.
  • Execute change controls and validation activities.
  • Collaborate with Manufacturing and Quality to resolve issues.
  • Provide on-call support for GMP manufacturing operations.
  • Drive continuous improvements for reliability and compliance.
  • Maintain SOPs, procedures, and system records per FDA/GMP.

Kenntnisse

Automation programming
Troubleshooting
Cross-functional collaboration
Documentation and validation

Ausbildung

Bachelor's degree in Engineering, Computer Science, or related technical field

Tools

DeltaV
OSI PI
PLC
SCADA/HMI
DCS platforms

Jobbeschreibung

Novartis Group of Companies in Durham, NC is seeking an Automation Engineer III focused on compounding, CIP, SIP and utility distribution to help ensure compliant, reliable pharmaceutical manufacturing.

You will troubleshoot, implement improvements, support validation, and collaborate with Manufacturing and Quality across the site. This onsite role requires a Bachelor's degree and 5+ years GMP experience with DeltaV, OSI PI, PLC/SCADA.

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