Senior Biopharma Manufacturing Systems Engineer (Automation)

Amgen Inc. (IR)

Juncos (PR)

On-site

USD 110,000 - 160,000

Full time

5 days ago
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Benefits offered by this job

Retirement and Savings Plan
Medical, dental & vision coverage
Life & disability insurance
Annual bonus program
Stock-based long-term incentives
Flexible work models

Job summary

Amgen Inc. is seeking a Senior Manufacturing Systems Engineer (Automation) to advance automation reliability and digital transformation in biopharmaceutical manufacturing.

You will focus on AVEVA Wonderware Intouch and Rockwell PLC/SCADA integration, ensuring cGMP compliance, data integrity, and lifecycle ownership across projects. The role involves leading automation design, validation, and change-control activities, collaborating with cross-functional teams, and driving continuous improvement

Qualifications

  • Advanced degree in engineering required with relevant manufacturing automation experience.
  • Experience with regulated manufacturing environments and systems.
  • Ability to lead automation lifecycle activities and capital projects.

Responsibilities

  • Serve as SME in manufacturing systems and digital technologies.
  • Lead MES/SCADA/PLC integration and related IT tier systems.
  • Collaborate with multifunctional teams to define system requirements.
  • Develop and maintain system documentation and test plans.
  • Troubleshoot system issues and coordinate with IT/vendor support.
  • Ensure compliance with cGMP, data integrity, and cybersecurity.

Skills

Automation systems
cGMP readiness
System documentation
Troubleshooting
Cross-functional collaboration

Education

Doctorate degree in Engineering
Master’s degree in Engineering with 2 years experience
Bachelor’s degree in Engineering with 4 years experience

Tools

AVEVA Wonderware Intouch
Rockwell Automation PLC/SCADA
OPC/DeviceNet/Ethernet/IP

Job description

Amgen Inc. is seeking a Senior Manufacturing Systems Engineer (Automation) to advance automation reliability and digital transformation in biopharmaceutical manufacturing.

You will focus on AVEVA Wonderware Intouch and Rockwell PLC/SCADA integration, ensuring cGMP compliance, data integrity, and lifecycle ownership across projects. The role involves leading automation design, validation, and change-control activities, collaborating with cross-functional teams, and driving continuous improvement

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