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, Automation, Controls, Electrical Engineering, Instrumentation, or related field.
  • 8+ years of experience in automation, controls, engineering, or related manufacturing environments.
  • Experience in GMP-regulated settings, specifically in pharmaceutical, biotech, or medical device industries.
  • Strong skills in project execution and managing stakeholder relationships.
  • Experience with commissioning, testing, qualification, or validation activities.

Responsibilities

  • Lead automation projects from design and planning through implementation and closeout.
  • Support modifications and improvements to building management systems and process automation systems.
  • Coordinate engineering design, integration, and implementation activities.
  • Develop and coordinate testing, commissioning, and validation activities.
  • Manage project schedules, including risks and change controls.
  • Ensure compliance with GMP, safety, quality, and site procedures.

Benefits

  • Dynamic work environment focused on innovation and collaboration.
  • Opportunities for professional development and career growth.
  • Supportive and purpose-driven team culture.
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

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

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#LI-ONSITE

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