Senior Automation Engineer

Validation and Engineering Group, Inc

$110K — $130K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or related field.
  • 8+ years of experience in automation or related environments.
  • Experience in pharmaceutical or GMP-regulated environments.
  • Strong project execution and stakeholder management skills.
  • Experience in commissioning and validation activities.

Responsibilities

  • Lead and manage automation projects from design to closeout.
  • Support modifications to various automation systems.
  • Coordinate engineering design and implementation activities.
  • Develop and oversee testing and validation processes.
  • Manage project schedules and address risks and issues.
  • Coordinate with stakeholders and vendors for project delivery.

Benefits

  • Collaborative work environment with engineering and operations teams.
  • Opportunity to lead critical automation projects.
  • Work in a dynamic, active manufacturing setting.
  • Exposure to advanced automation technologies and methodologies.
  • Potential for professional development and career growth.
Full Job Description
  • Senior Automation Engineer

Job Summary

We are seeking a Senior Automation Engineer to support an Automation Resilience Program in Rockville, MD.

The selected candidate will lead and coordinate automation engineering, implementation, testing, commissioning, validation support, documentation, and project closeout activities. The role will work closely with Engineering, Automation, Operations, Quality, Validation, IT, and external vendors.

Key Responsibilities
  • Lead automation projects from design and planning through implementation and closeout.
  • Support modifications and improvements to BMS, COPA-DATA Zenon (CDZ), EMS, PLCs, and process automation systems.
  • Coordinate engineering design, system integration, migration, controls modifications, and implementation activities.
  • Develop and coordinate testing, commissioning, and validation activities.
  • Support creation, execution, review, and approval of validation protocols in accordance with site requirements.
  • Manage project schedules, risks, issues, change controls, work orders, and action items.
  • Coordinate outages, shutdowns, dependencies, and implementation activities in an active manufacturing environment.
  • Ensure compliance with GMP, safety, quality, and site procedures.
  • Review and maintain engineering drawings, configuration records, test documentation, and as-built/turnover packages.
  • Coordinate with internal stakeholders, vendors, and subcontractors to ensure successful project delivery.
  • Proactively escalate risks impacting safety, compliance, schedule, quality, or operations.

Required Qualifications
  • Bachelor's degree in Engineering, Automation, Controls, Electrical Engineering, Instrumentation, or related field.
  • 8+ years of experience in automation, controls, engineering, or related manufacturing environments.
  • Experience supporting automation projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments.
  • Strong project execution and stakeholder management skills.
  • Experience with commissioning, testing, qualification, or validation activities.
  • Experience working in active manufacturing facilities with controlled implementation/outage requirements.

Preferred Experience
  • Siemens Desigo / BMS
  • COPA-DATA Zenon
  • Rockwell PLC / Controls
  • Environmental Monitoring Systems (EMS)
  • Process automation and system integration
  • PLC/control system migration
  • Automation architecture and data historization
  • GMP computerized systems
  • Commissioning and qualification

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