Automation Project Manager

Reposted 3 Days Ago
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Rockville, MD, USA
In-Office
Senior level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Lead automation projects for design, implementation, testing, commissioning, validation support, and closeout in a GMP-regulated manufacturing environment. Coordinate system integration, PLC and BMS/Zenon/EMS modifications and migrations, manage schedules, risks, outages, and stakeholder/vendor coordination while ensuring compliance with safety, quality, and site procedures.
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:

  • Automation Project Manager

Job Summary

We are seeking a Automation Project Manager 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.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

#LI-LN1

#LI-ONSITE

Skills Required

  • 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.
  • Siemens Desigo / BMS experience.
  • COPA-DATA Zenon experience.
  • Rockwell PLC / Controls experience.
  • Environmental Monitoring Systems (EMS) experience.
  • Experience with PLC/control system migration, automation architecture, and data historization.
  • Familiarity with GMP computerized systems and commissioning/qualification processes.
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The Company
HQ: Geneva
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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