Automation Systems Engineer — Remote-Eligible & Impactful

BioSpace

Holly Springs (NC)

Hybrid

USD 110.000 - 140.000

Vollzeit

vor 39 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Remote work arrangements
Flexible work models

Zusammenfassung

Amgen North Carolina is seeking a Manufacturing Systems Engineer in Automation to join the Facilities & Engineering Automation team. You will build and maintain automation systems for the new drug substance plant, collaborating with engineers and stakeholders to deliver robust process control and compliant documentation.

You will support QA/good manufacturing practices, perform validations, and drive continuous improvement across operations, ensuring safety and efficiency in a fast-paced

Qualifikationen

  • Requires a degree in engineering with relevant experience in automation.
  • Experience with GMP biopharmaceutical production facilities is preferred.
  • Strong documentation, QA support, and validation experience required.

Aufgaben

  • Develop and maintain process control on Emerson DeltaV DCS.
  • Collaborate with stakeholders to translate process requirements into automation solutions.
  • Provide documentation for delivered solutions and processes.
  • Support QA in computerized systems validation in a GxP environment.
  • Perform Data Integrity Assessments per Amgen and industry standards.
  • Support design alignment with specifications and safety requirements.
  • Assist with vendor FAT and commissioning/qualification activities.
  • Maintain engineering documentation and SOPs.

Kenntnisse

Cross-functional collaboration
Technical writing
Communication skills
Self-directed

Ausbildung

Bachelor's Degree in Engineering
Master's Degree
Associates Degree
High School Diploma / GED

Tools

Emerson DeltaV DCS
OPC
Foundation Fieldbus
Profibus

Jobbeschreibung

Amgen North Carolina is seeking a Manufacturing Systems Engineer in Automation to join the Facilities & Engineering Automation team. You will build and maintain automation systems for the new drug substance plant, collaborating with engineers and stakeholders to deliver robust process control and compliant documentation.

You will support QA/good manufacturing practices, perform validations, and drive continuous improvement across operations, ensuring safety and efficiency in a fast-paced

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