Senior DeltaV Automation Engineer – Drug Substance Ops

Amgen Inc.

Holly Springs (NC)

On-site

USD 137,000 - 185,000

Full time

4 days ago
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Job summary

Amgen Inc. in North Carolina is seeking a Senior Manufacturing Systems Engineer focused on downstream automation and DeltaV DCS for the new drug substance manufacturing facility.

You will lead automation engineers, collaborate with capital projects, and deliver robust process automation in a fast-paced GMP environment. The role emphasizes ownership of change controls, CAPAs, and deviations, with responsibilities spanning IV/ACO support, documentation, and cross-functional collaboration to

Qualifications

  • High School Diploma / GED and 10 years of Engineering experience OR
  • Associate’s Degree and 8 years of Engineering experience OR
  • Bachelor’s Degree and 4 years of Engineering experience OR
  • Master’s Degree and 2 years of Engineering experience OR
  • Doctorate Degree

Responsibilities

  • Provide automation leadership to engineers supporting GMP Drug Substance Plant Operations
  • Collaborate with capital projects to deliver robust process automation systems
  • Develop and maintain DeltaV distributed control system (DCS)
  • Work with process SMEs to translate requirements into digital automated solutions
  • Ensure documentation and validation compliance in a GxP environment

Skills

Automation leadership
Process control
GMP knowledge
Analytical problem solving
Project management
Technical documentation

Education

Bachelor’s Degree in Engineering
Associate’s Degree in Engineering
Master’s Degree in Engineering
Doctorate Degree
Electrical/Biotech Engineering

Tools

Emerson DeltaV
OPC
Foundation Fieldbus
Profibus
DeviceNet
DeltaV Live

Job description

Amgen Inc. in North Carolina is seeking a Senior Manufacturing Systems Engineer focused on downstream automation and DeltaV DCS for the new drug substance manufacturing facility.

You will lead automation engineers, collaborate with capital projects, and deliver robust process automation in a fast-paced GMP environment. The role emphasizes ownership of change controls, CAPAs, and deviations, with responsibilities spanning IV/ACO support, documentation, and cross-functional collaboration to

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