Lead planning, coordination, readiness, and execution of complex cybersecurity verification and validation activities across large-scale data center construction and commissioning programs.
Responsibilities
Coordinate activities across construction teams, commissioning organizations, data center operations, controls and automation teams, OEMs, system integrators, network teams, cybersecurity specialists, and independent Cybersecurity Commissioning Agents
Align all sites with integrated program plans covering cybersecurity verification and validation, construction, commissioning, operational readiness, and technical dependencies
Coordinate activities across multiple geographic regions, sites, delivery teams, and Cybersecurity commissioning agents
Maintain visibility of site readiness, schedules, dependencies, risks, constraints, and required technical resources
Maintain program-level schedule, effort, resource utilization, budget, and financial health tracking
Requirements
Bachelor's or higher in Electrical, Controls, Automation, Mechanical, Network, Computer, Systems engineering or related field
Nice to have: PMP or PgMP
Nice to have: CxA, CCP, CBCP or equivalent commissioning credentials
Nice to have: CISSP, GICSP, IEC 62443 cybersecurity certification
Nice to have: Experience with Schneider Electric, Siemens, Rockwell Automation, ABB, Honeywell, Johnson Controls
Lead and execute automation activities that support pilot-scale GMP manufacturing campaigns for bulk biologics, including vaccines and therapeutic proteins used in clinical development.
Locations (3)
West Point, Pennsylvania, United States
San Francisco, California, United States
Los Angeles, California, United States
Compensation
The salary range for the primary location of this role is: $117,000.00 - $184,200.00
Responsibilities
Provide technical leadership and ongoing support for facility automation systems.
Serve as the automation subject matter expert for GMP clinical manufacturing campaigns.
Lead and/or execute the integration, commissioning, qualification, and startup of new equipment and automation projects.
Author, review, and approve GMP documentation, including change controls, test protocols, SDLC documentation, SOPs, safety assessments, deviation investigations and corrective actions.
Senior Specialist - Biologics Pilot Plant Automation Engineer (On-site)Merck · West Point, US+2 more