Senior Automation Engineer

Posted 6 Days Ago
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Rockville, MD, USA
In-Office
Senior level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Supports automation engineering across design, system integration, programming, testing, commissioning, validation, troubleshooting, migration, and documentation in GMP-regulated manufacturing environments. Works with BMS, Zenon, EMS, PLCs, and process automation systems while coordinating with engineering, quality, validation, IT, operations, vendors, and project teams. Ensures compliance with GMP, safety, data integrity, and site procedures, and provides technical support during outages and system implementations.
Summary Generated by Built In

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • 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 provide technical automation engineering support for system modifications, integration, implementation, testing, commissioning, validation, troubleshooting, and documentation activities. The role will work closely with the Automation Project Manager, Engineering, Automation, Operations, Quality, Validation, IT, and external vendors.

Key Responsibilities

  • Provide automation engineering support from design and planning through implementation, testing, commissioning, and closeout.

  • Support modifications and improvements to BMS, COPA-DATA Zenon (CDZ), EMS, PLCs, and process automation systems.

  • Support engineering design, system integration, migration, controls modifications, and implementation activities.

  • Perform and support automation system configuration, programming, testing, troubleshooting, and technical issue resolution.

  • Support testing, commissioning, and validation activities.

  • Support creation, execution, review, and approval of validation protocols in accordance with site requirements.

  • Provide technical support during system outages, shutdowns, migrations, and implementation activities in an active manufacturing environment.

  • Ensure automation activities comply with GMP, safety, quality, data integrity, and site procedures.

  • Review and maintain engineering drawings, configuration records, control documentation, test documentation, and as-built/turnover packages.

  • Work with internal stakeholders, vendors, system integrators, and subcontractors throughout project execution.

  • Identify and communicate technical risks, issues, dependencies, and potential impacts to safety, compliance, schedule, quality, or operations.

  • Support troubleshooting and resolution of automation, controls, communications, and system integration issues.

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 systems and projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments.

  • Hands-on experience with automation and controls system design, configuration, integration, testing, or troubleshooting.

  • Experience with commissioning, testing, qualification, or validation activities.

  • Working knowledge of GMP requirements and computerized systems in regulated manufacturing environments.

  • Experience working in active manufacturing facilities with controlled implementation and outage requirements.

  • Strong technical problem-solving, communication, documentation, and cross-functional collaboration skills.

  • Ability to work on site in Rockville, MD and remain actively engaged with project and site teams.

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.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation,

Skills Required

  • Bachelor's degree in Engineering, Automation, Controls, Electrical Engineering, Instrumentation, or a related field
  • 8 or more years of experience in automation, controls, engineering, or related manufacturing environments
  • Experience supporting automation systems and projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments
  • Hands-on experience with automation and controls system design, configuration, integration, testing, or troubleshooting
  • Experience with commissioning, testing, qualification, or validation activities
  • Working knowledge of GMP requirements and computerized systems in regulated manufacturing environments
  • Experience working in active manufacturing facilities with controlled implementation and outage requirements
  • Strong technical problem-solving, communication, documentation, and cross-functional collaboration skills
  • Ability to work on site in Rockville, Maryland and remain actively engaged with project and site teams
  • Experience with Siemens Desigo or building management systems
  • Experience with COPA-DATA Zenon
  • Experience with Rockwell PLC or controls systems
  • Experience with environmental monitoring systems
  • Experience with process automation and system integration
  • Experience with PLC or control system migration
  • Experience with automation architecture and data historization
  • Experience with GMP computerized systems
  • Experience with commissioning and qualification
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The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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