Regeneron · 1 day ago
Laboratory Equipment IT Engineer, Regeneron Cell Medicines
Cambridge, MA
Full-time
Onsite
Mid Level
$79K/yr - $129K/yr
3+ years expRegeneron is advancing cell therapies and combination approaches in oncology and immunology, and they are seeking a motivated Laboratory Equipment IT Engineer. This role involves supporting and maintaining critical systems for Clinical Manufacturing and R&D, ensuring compliance, and enhancing automation processes.
BiopharmaBiotechnologyPharmaceutical
Responsibilities
Supporting all manufacturing and QC equipment within RCM’s 30,000 SF Phase 1 clinical manufacturing facility
Maintaining System documentation, including converting User Requirement Specifications to a Detail Design Specification, writing Configuration Test Plans, and summary reports
Leading IT Applications systems security access and periodic audit trail reviews
Performing investigations relating to manufacturing deviations and anomalies associated with automation systems and control system software
Support engineering and validation projects as well as provide support to manufacturing activities with process control and process monitoring equipment software design, commissioning, and testing to meet end user requirements
Supporting automation activities by updating/authoring system specifications, user and functional requirements specifications, as well as generating and implementing necessary FAT and SAT protocols
Designing and developing test plans and implementing software/hardware improvements to automated process control and process monitoring equipment according to change control procedures
Ensuring systems' data is backed up / archived as required to ensure system can meet defined RTO and RPO; perform recovery of data as needed
Creating and maintaining configuration specifications for cGMP software for process control, monitoring and testing
Ensuring systems remain in compliant state including process change control requests for system configurations, including requirement and/or design specifications, test plans, technical evaluation and quality risk assessments
Supporting system integration with existing systems (ex. LIMS, Historian) as required by business needs
Qualification
Required
Bachelor's degree in Information Technology or related field
3-5 years of relevant experience in a manufacturing/lab/IT setting
Experience in a pharmaceutical or biopharmaceutical manufacturing facility
Preferred
Experience working in a GMP environment is very advantageous
Experience with automated systems for environmental monitoring and compliance; Rees is preferred
Benefits
Health and wellness programs
Fitness centers
Equity awards
Annual bonuses
Paid time off for eligible employees at all levels
Company
Regeneron
Regeneron Pharmaceuticals specializes in the discovery, development, and commercialization of innovative medicines.
10001+ employees
H1B Sponsorship
Regeneron has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (157)
2024 (128)
2023 (128)
2022 (137)
2021 (104)
2020 (122)
Funding
Current Stage
Public CompanyTotal Funding
$15.93MKey Investors
U.S. Department of Health & Human Services
2024-07-11Post Ipo Equity· $2.03M
2023-10-18Post Ipo Equity· $5M
2016-08-22Post Ipo Equity· $8.9M
Leadership Team
Aris Baras
Senior Vice President, Regeneron Pharmaceuticals, General Manager, Regeneron Genetics Center
Bari Kowal
Senior Vice President, Head Development Operations & Portfolio Management
Recent News
2026-01-13
2026-01-09
Company data provided by crunchbase