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Engineer III, Automation

Biogen
Full-time
Remote friendly (Triangle, NC)
United States
$75,000 - $98,000 USD yearly
Operations

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Role Summary

Engineer III, Automation. Motivated Automation Engineer to support administration, reliability, and continuous improvement of GMP-critical automation platforms enabling large-scale biologics production. Hands-on experience across automation technologies and cross-functional engagement with Manufacturing, Quality, Facilities/Utilities, and IT.

Responsibilities

  • Provide daily administration, monitoring, and troubleshooting for the site’s Batch Control System (Emerson DeltaV).
  • Support Single-Use Bioreactor operations by administering and maintaining TruBio control platforms.
  • Maintain and configure the Manufacturing Data Historian and contextualization layers (OSIsoft PI, PI Vision, interfaces, and AF).
  • Support InfoBatch batch reporting integrations, configuration updates, and troubleshooting.
  • Administer Building Management and Alarm Management platforms including FactoryTalk, TiPS, and TopView.
  • Support Syncade system and database administration activities.
  • Participate in automation upgrade projects, system hardening, patching, and lifecycle planning.
  • Assist in designing, testing, documenting, and implementing system changes following GMP and validation requirements.
  • Support system migrations, virtualization initiatives, server upgrades, and integration with IT infrastructure.
  • Provide support as needed for manufacturing operations.
  • Troubleshoot equipment, network, and software issues involving PLC, HMIs, historians, MES, and batch control systems.
  • Work with cross-functional teams to diagnose and resolve automation-related deviations.
  • Create and maintain system documentation, including user accounts, SOPs, configurations, and validation documentation.
  • Ensure automation systems remain audit-ready and compliant with regulatory and corporate standards.

Qualifications

  • Required: Bachelor’s degree in Engineering (Chemical, Electrical, Mechanical, or related field).
  • Required: 2–4 years of experience supporting automation or control systems in biotechnology, pharmaceutical, or regulated manufacturing environments.
  • Required: Experience with at least one of DeltaV, TruBio, PI, InfoBatch, FactoryTalk, Syncade, or equivalent industrial automation platforms.
  • Required: Basic working knowledge of control system networks (VLANs, firewalls, virtual machines, domain/LDAP authentication).
  • Required: Demonstrated ability to troubleshoot complex system interactions across multiple layers of automation architecture.
  • Required: Comfortable collaborating with teams outside of Automation – Process Engineering, Validation, Quality, etc.
  • Preferred: Experience in GMP-regulated manufacturing environments.
  • Preferred: Familiarity with batch control logic, S88, 21 CFR Part 11, and data integrity principles.
  • Preferred: Knowledge of server management, virtualization (Nutanix, VMware), or Windows Server administration.
  • Preferred: Experience with scripting or automation tools (PowerShell, Python, SQL).

Skills

  • Problem solving and ownership of projects
  • Cross-functional collaboration
  • Automation system administration and troubleshooting
  • Documentation and validation maintenance

Education

  • Bachelor’s degree in Engineering (Chemical, Electrical, Mechanical, or related field)

Additional Requirements

  • None beyond listed qualifications.
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