Principal Automation Systems Administrator, Manufacturing & Lab Support
Regeneron
August 21, 2026
On-site
Menands, NY
IT
Responsibilities:
- Develop system hardware/software specifications, code, and networking configurations/standards to meet cGMP and procedural requirements across IOPS
- Provide advanced technical automation support, troubleshooting, and investigations per SOPs, GAMP 5, and departmental practices
- Lead SAT/FAT, validation, qualification, and improvement efforts; manage interdepartmental/global projects for corrective actions, software/hardware improvement, and new equipment/infrastructure
- Author/review Software Lifecycle Documentation, SOPs, Change Controls, EOEs/NOEs/DNFs, risk assessments, impact statements, and CAPA plans
- Serve as technical liaison between Automation and the business; identify alternative solutions and drive continuous improvement in processes/procedures/architecture standards
- Support selection/assessment of automation partners and vendors; manage vendor relationships and deliverables
- Provide training/mentoring to Engineering/Automation and external departments; may supervise/mentor direct reports/contractors
Qualifications (Required/Preferred):
- BS/BA in Science, Engineering, or related field
- Principal Automation Systems Administrator: 8+ years relevant experience (or Staff level: 10+ years relevant experience)
- Equivalent combination of education/experience may be considered
- Preferred: direct experience in pharmaceutical/biopharmaceutical manufacturing facility
- Advanced: configuring/troubleshooting control, monitoring, and product release testing systems (design/install)
- Advanced: troubleshooting network infrastructure and server-based systems
- Current knowledge of cGMP biotech/pharma operations, regulatory/quality policies and documentation methods
- Strong project management; ability to lead changing priorities
Cleanroom/Physical Requirements:
- Full cleanroom attire; remove jewelry/makeup/nail adornments
- Ability to perform physical requirements for up to 10 hours in a clean room; may include lifting/pushing/pulling up to 50 lbs
Application Instructions:
- Apply now
- Develop system hardware/software specifications, code, and networking configurations/standards to meet cGMP and procedural requirements across IOPS
- Provide advanced technical automation support, troubleshooting, and investigations per SOPs, GAMP 5, and departmental practices
- Lead SAT/FAT, validation, qualification, and improvement efforts; manage interdepartmental/global projects for corrective actions, software/hardware improvement, and new equipment/infrastructure
- Author/review Software Lifecycle Documentation, SOPs, Change Controls, EOEs/NOEs/DNFs, risk assessments, impact statements, and CAPA plans
- Serve as technical liaison between Automation and the business; identify alternative solutions and drive continuous improvement in processes/procedures/architecture standards
- Support selection/assessment of automation partners and vendors; manage vendor relationships and deliverables
- Provide training/mentoring to Engineering/Automation and external departments; may supervise/mentor direct reports/contractors
Qualifications (Required/Preferred):
- BS/BA in Science, Engineering, or related field
- Principal Automation Systems Administrator: 8+ years relevant experience (or Staff level: 10+ years relevant experience)
- Equivalent combination of education/experience may be considered
- Preferred: direct experience in pharmaceutical/biopharmaceutical manufacturing facility
- Advanced: configuring/troubleshooting control, monitoring, and product release testing systems (design/install)
- Advanced: troubleshooting network infrastructure and server-based systems
- Current knowledge of cGMP biotech/pharma operations, regulatory/quality policies and documentation methods
- Strong project management; ability to lead changing priorities
Cleanroom/Physical Requirements:
- Full cleanroom attire; remove jewelry/makeup/nail adornments
- Ability to perform physical requirements for up to 10 hours in a clean room; may include lifting/pushing/pulling up to 50 lbs
Application Instructions:
- Apply now