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Laboratory Equipment IT Engineer, Regeneron Cell Medicines, Cambridge
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Client:
Location:
Cambridge, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
6892504e8e0f
Job Views:
5
Posted:
29.06.2025
Expiry Date:
13.08.2025
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Job Description:
We are seeking a motivated Laboratory Equipment IT Engineer to support and maintain Building Management, Clinical Manufacturing Equipment and data acquisition/monitoring systems that support Clinical Manufacturing and Research and Development (R&D). This role is a part of Regeneron Cell Medicines (RCM), a newly formed R&D unit within Regeneron to advance cell therapies and combination approaches in oncology and immunology. We hope you are excited to serve as the technical SME as well as operate at the system administration, engineering, and management levels.
As an Laboratory Equipment IT Engineer, a typical day might include the following:
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
This role might be for you if you:
You enjoy working in a fast-paced environment and can be flexible with changing priorities
You thrive in a team-based, multi-functional, collaborative environment
You possess a problem-solving mentality
You have excellent verbal and written communication skills
In order to be considered for this role, you must have at least a Bachelor's degree in Information Technology or related field and 3-5 years of relevant experience in a manufacturing/lab/IT setting. Must have experience in a pharmaceutical or biopharmaceutical manufacturing facility. Must have experience with automated systems for environmental monitoring and compliance; Rees is preferred. Experience working in a GMP environment is very advantageous.
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