Automation Engineer II/III - DeltaV & Syncade Expert

Biogen

North Carolina

On-site

USD 77,000 - 100,000

Full time

4 days ago
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Benefits offered by this job

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Fitness reimbursement
Paid vacation
Paid holidays
401(k) match
Employee stock purchase plan
Tuition reimbursement

Job summary

Biogen’s RTP Bio site seeks an Automation Engineer II/III to support DeltaV DCS and Syncade MES systems. You will craft software, validate changes, and ensure reliable integration with PI Historian, Oracle, CMMS, Veeva, and Labware (LIMS).

This role emphasizes continuous improvement and rigorous quality standards in a fast-paced biopharmaceutical environment. You will lead small to mid-sized projects, collaborate across functions, and contribute to the site’s automation strategy while

Qualifications

  • Bachelor's degree in engineering from an accredited college.
  • Engineer II requires 2+ years of experience in MES/DCS environments.
  • Experience with MES validation, change controls, and troubleshooting.

Responsibilities

  • Configure and maintain DeltaV DCS and Syncade MES software to support process improvements and new equipment implementations.
  • Author, review, and approve MES and DeltaV DCS documentation and validation deliverables.
  • Create and execute software testing scripts and support validation activities per GAMP 5.
  • Execute and manage change controls while ensuring compliance with site procedures and quality requirements.
  • Troubleshoot MES and DCS issues during testing and manufacturing operations; participate in on-call rotations.

Skills

MES recipe authoring
DeltaV DCS
Troubleshooting
Validation
Cross-functional collaboration

Education

Bachelor's degree in Engineering

Tools

Syncade MES
DeltaV DCS
PI Historian

Job description

Biogen’s RTP Bio site seeks an Automation Engineer II/III to support DeltaV DCS and Syncade MES systems. You will craft software, validate changes, and ensure reliable integration with PI Historian, Oracle, CMMS, Veeva, and Labware (LIMS).

This role emphasizes continuous improvement and rigorous quality standards in a fast-paced biopharmaceutical environment. You will lead small to mid-sized projects, collaborate across functions, and contribute to the site’s automation strategy while

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