Principal Automation Integration Engineer

Regeneron Pharmaceuticals • Town of Colonie, NY

1d • Onsite

About The Position

We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. As a Principal Automation Systems Integration Engineer, a typical day might include the following: Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. Supporting small manufacturing, engineering, and validation projects. Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure Creation, modification, and maintenance of automation system documentation

Requirements

• Experience with OT applications, including SCADAs, HMIs, Historians, etc.
• Familiarity with standing up large systems at the enterprise level
• Core knowledge related to ISE S95 and S88 principles and IT/Automation integration
• Familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure
• Bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering
• 8+ years of relevant experience

Nice To Haves

• Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better
• Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly
• Can balance changing priorities with increasing workload by making/communicating timely decisions

Responsibilities

• Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures.
• Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems.
• Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines.
• Supporting small manufacturing, engineering, and validation projects.
• Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action.
• Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols.
• Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure
• Creation, modification, and maintenance of automation system documentation

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Number of Employees: 5,001-10,000 employees