Onsite Automation Lead — GMP Biopharma Systems

Catalent, Inc.

Harmans (MD)

Vor Ort

USD 120.000 - 140.000

Vollzeit

vor 23 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical, dental and vision benefits
Tuition Reimbursement
8 paid holidays

Zusammenfassung

Catalent, Inc. is seeking a Senior Automation Engineer in Harmans, MD, onsite. The role leads troubleshooting of PLCs, SCADA/HMI, historians, alarms, and networks, and drives automation workstreams for major changes and capital projects. You will mentor junior engineers and ensure cGMP compliance.

Requires 5–8 years in GMP automation, strong project leadership, and experience with change controls and CAPAs. Excellent collaboration with Quality and Validation teams is essential.

Qualifikationen

  • Bachelor’s degree or Associate degree with relevant experience in GMP environments.
  • 5+ years supporting automation systems in GMP manufacturing.

Aufgaben

  • Serve as system owner and automation SME.
  • Troubleshoot PLC/SCADA/HMI, historians, alarms, and networks.
  • Lead automation workstreams for capital projects and changes.
  • Author/change controls, deviations, CAPAs, and lifecycle docs.

Kenntnisse

PLC
SCADA/HMI
Historians
Automation projects
Change controls
Regulated environments
Troubleshooting
Root cause investigations

Ausbildung

Bachelor’s degree in Engineering or related field
Associate degree in related field

Tools

SCADA/HMI
Historians
Industrial networks
Alarms

Jobbeschreibung

Catalent, Inc. is seeking a Senior Automation Engineer in Harmans, MD, onsite. The role leads troubleshooting of PLCs, SCADA/HMI, historians, alarms, and networks, and drives automation workstreams for major changes and capital projects. You will mentor junior engineers and ensure cGMP compliance.

Requires 5–8 years in GMP automation, strong project leadership, and experience with change controls and CAPAs. Excellent collaboration with Quality and Validation teams is essential.

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