Automation Manager: Lead cGMP Systems & Team

BioSpace; City of Rensselaer (NY); On-site; USD 103,000 - 198,000; Full time

Job summary

Regeneron is seeking an Automation Manager to lead a team responsible for cGMP automation quality systems, software change control, and corrective actions. You will coach automation professionals, develop procedures, and ensure manufacturing systems operate reliably while delivering timely fixes.

The role emphasizes mentoring, process improvements, and collaboration with engineering and manufacturing to maintain compliance and performance in a fast-growing biopharma environment.

Qualifications

• BS/BA in Engineering or related field.
• 6+ years in automation for Associate Manager level or 7+ years for Manager level.
• 1 to 3+ years of supervisory experience, depending on level.
• 1+ year in design, installation, maintenance, or troubleshooting of automated control systems.
• Knowledge of cGMP software quality principles, data integrity regulations.
• Experience with PLC/HMI in industrial settings.
• Familiarity with Allen-Bradley and Siemens PLC platforms and manufacturing networks.

Responsibilities

• Manage performance, training, and results of the automation team.
• Provide technical and automation support to manufacturing.
• Oversee configuration and support of process equipment and cGMP software administration.
• Prepare periodic evaluation reports for automated systems used in manufacturing.
• Investigation of deviations and anomalies related to automation and software.
• Lead projects related to corrective action or equipment performance improvement.
• Implement change control procedures and protocols.
• Support validation with design reviews, software testing, and protocol review.

Skills

Supervisory experience

Automation systems knowledge

PLC/HMI experience

Regulatory compliance knowledge

Education

BS/BA in Engineering

Tools

Allen-Bradley PLC

Siemens PLC

Manufacturing Execution Systems (MES)

Job description

Regeneron is seeking an Automation Manager to lead a team responsible for cGMP automation quality systems, software change control, and corrective actions. You will coach automation professionals, develop procedures, and ensure manufacturing systems operate reliably while delivering timely fixes.

The role emphasizes mentoring, process improvements, and collaboration with engineering and manufacturing to maintain compliance and performance in a fast-growing biopharma environment.